728913 chr6:70925774:G>A COL9A1 NM_078485:c.*826C>T THREE_PRIME_EXON Unknown significance rs533440374 This variant is a VUS because it does not have enough information. 728914 chr6:70925791:C>T COL9A1 NM_078485:c.*809G>A THREE_PRIME_EXON Unknown significance rs557539788 This variant is a VUS because it does not have enough information. 728915 chr6:70925954:A>G COL9A1 NM_078485:c.*646T>C THREE_PRIME_EXON Unknown significance rs746120474 This variant is a VUS because it does not have enough information. 728916 chr6:70926001:T>C COL9A1 NM_078485:c.*599A>G THREE_PRIME_EXON Unknown significance rs551683531 This variant is a VUS because it does not have enough information. 728917 chr6:70926042:C>T COL9A1 NM_078485:c.*558G>A THREE_PRIME_EXON Benign rs373018250 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 0 1322 0 0 1006 0 0 694 0 0 1008 0 6 978 0.0061 6 5008 0.00119808 728918 chr6:70926050:A>C COL9A1 NM_078485:c.*550T>G THREE_PRIME_EXON Unknown significance rs560557089 This variant is a VUS because it does not have enough information. 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 728919 chr6:70926059:G>A COL9A1 NM_078485:c.*541C>T THREE_PRIME_EXON Unknown significance rs191432958 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361 728920 chr6:70926062:A>T COL9A1 NM_078485:c.*538T>A THREE_PRIME_EXON Benign rs55709776 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 8 1322 0.0061 0 1006 0 0 694 0 0 1008 0 0 978 0 8 5008 0.00159744 728921 chr6:70926070:C>T COL9A1 NM_078485:c.*530G>A THREE_PRIME_EXON Unknown significance rs570034842 This variant is a VUS because it does not have enough information. 728922 chr6:70926097:C>T COL9A1 NM_078485:c.*503G>A THREE_PRIME_EXON Unknown significance rs375176049 This variant is a VUS because it does not have enough information. 728923 chr6:70926126:T>C COL9A1 NM_078485:c.*474A>G THREE_PRIME_EXON Unknown significance rs780122438 This variant is a VUS because it does not have enough information. 728924 chr6:70926172:ATA>- COL9A1 NM_078485:c.*428_*432delTAT THREE_PRIME_EXON Unknown significance rs751855141 This variant is a VUS because it does not have enough information. 728925 chr6:70926175:A>G COL9A1 NM_078485:c.*425T>C THREE_PRIME_EXON Unknown significance rs749364459 This variant is a VUS because it does not have enough information. 728926 chr6:70926188:T>C COL9A1 NM_078485:c.*412A>G THREE_PRIME_EXON Unknown significance rs186882898 This variant is a VUS because it does not have enough information. 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 728927 chr6:70926220:T>C COL9A1 NM_078485:c.*380A>G THREE_PRIME_EXON Unknown significance rs771960432 This variant is a VUS because it does not have enough information. 728928 chr6:70926225:C>T COL9A1 NM_078485:c.*375G>A THREE_PRIME_EXON Unknown significance rs531745614 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 728929 chr6:70926235:C>G COL9A1 NM_078485:c.*365G>C THREE_PRIME_EXON Unknown significance rs191406921 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 3 5008 0.000599042 728930 chr6:70926240:C>T COL9A1 NM_078485:c.*360G>A THREE_PRIME_EXON Unknown significance rs565189871 This variant is a VUS because it does not have enough information. 1 1322 0.0008 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 3 5008 0.000599042 728931 chr6:70926334:A>G COL9A1 NM_078485:c.*266T>C THREE_PRIME_EXON Benign rs1064250 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 611 1322 0.4622 416 1006 0.4135 269 694 0.3876 269 1008 0.2669 417 978 0.4264 1982 5008 0.395767 728934 chr6:70926357:C>T COL9A1 NM_078485:c.*243G>A THREE_PRIME_EXON Unknown significance rs201244576 This variant is a VUS because it does not have enough information. 728932 chr6:70926358:->T COL9A1 NM_078485:c.*242_*243insA THREE_PRIME_EXON Benign rs555755721 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 277 1322 0.2095 236 1006 0.2346 242 694 0.3487 347 1008 0.3442 215 978 0.2198 1317 5008 0.262979 728933 chr6:70926358:->TT COL9A1 NM_078485:c.*242_*243insAA THREE_PRIME_EXON Unknown significance rs555755721 This variant is a VUS because it does not have enough information. 728935 chr6:70926361:->GG COL9A1 NM_078485:c.*239_*240insCC THREE_PRIME_EXON Unknown significance rs796116774 This variant is a VUS because it does not have enough information. 728936 chr6:70926371:A>G COL9A1 NM_078485:c.*229T>C THREE_PRIME_EXON Benign rs2459555 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 288 1322 0.2179 46 1006 0.0457 27 694 0.0389 7 1008 0.0069 61 978 0.0624 429 5008 0.0856629 728937 chr6:70926404:A>G COL9A1 NM_078485:c.*196T>C THREE_PRIME_EXON Unknown significance rs770787617 This variant is a VUS because it does not have enough information. 728938 chr6:70926426:A>G COL9A1 NM_078485:c.*174T>C THREE_PRIME_EXON Unknown significance rs776515044 This variant is a VUS because it does not have enough information. 728939 chr6:70926435:C>G COL9A1 NM_078485:c.*165G>C THREE_PRIME_EXON Unknown significance rs759272502 This variant is a VUS because it does not have enough information. 728940 chr6:70926443:T>C COL9A1 NM_078485:c.*157A>G THREE_PRIME_EXON Unknown significance rs567006253 This variant is a VUS because it does not have enough information. 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361 728941 chr6:70926511:C>T COL9A1 NM_078485:c.*89G>A THREE_PRIME_EXON Unknown significance rs373398023 This variant is a VUS because it does not have enough information. 728942 chr6:70926552:C>T COL9A1 NM_078485:c.*48G>A THREE_PRIME_EXON Unknown significance rs373931410 This variant is a VUS because it does not have enough information. 0 8600 0 1 4406 0.000226963 1 13006 7.68876e-05 1 10132 9.86972e-05 0 11398 0 0 8474 0 0 6532 0 0 65368 0 0 884 0 0 16280 0 1 119068 8.39856e-06 728943 chr6:70926554:T>C COL9A1 NM_078485:c.*46A>G THREE_PRIME_EXON Unknown significance rs750975498 This variant is a VUS because it does not have enough information. 0 10132 0 0 11408 0 0 8480 0 0 6534 0 0 65424 0 0 888 0 1 16292 6.13798e-05 1 119158 8.39222e-06 728944 chr6:70926562:G>T COL9A1 NM_078485:c.*38C>A THREE_PRIME_EXON Unknown significance rs759522163 This variant is a VUS because it does not have enough information. 0 10134 0 0 11408 0 0 8490 0 0 6534 0 4 65458 6.11079e-05 0 888 0 0 16306 0 4 119218 3.3552e-05 728945 chr6:70926563:C>T COL9A1 NM_078485:c.*37G>A THREE_PRIME_EXON Unknown significance rs535973057 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361 0 10138 0 1 11406 8.76732e-05 0 8486 0 2 6536 0.000305998 1 65468 1.52746e-05 0 888 0 11 16300 0.000674847 15 119222 0.000125816 728946 chr6:70926564:G>A COL9A1 NM_078485:c.*36C>T THREE_PRIME_EXON Unknown significance rs6923452 This variant is a VUS because it does not have enough information. 3 8600 0.000348837 0 4406 0 3 13006 0.000230663 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 0 10146 0 0 11418 0 1 8496 0.000117702 0 6540 0 4 65492 6.10762e-05 0 886 0 0 16310 0 5 119288 4.19154e-05 728947 chr6:70926572:T>G COL9A1 NM_078485:c.*28A>C THREE_PRIME_EXON Unknown significance rs371413126 This variant is a VUS because it does not have enough information. 1 8600 0.000116279 0 4406 0 1 13006 7.68876e-05 728948 chr6:70926574:CAGA>- COL9A1 NM_078485:c.*26_*31delTCTG THREE_PRIME_EXON Unknown significance rs779371541 This variant is a VUS because it does not have enough information. 728949 chr6:70926575:A>G COL9A1 NM_078485:c.*25T>C THREE_PRIME_EXON Unknown significance rs755948864 This variant is a VUS because it does not have enough information. 0 10192 0 2 11440 0.000174825 0 8514 0 0 6558 0 0 65734 0 0 890 0 0 16328 0 2 119656 1.67146e-05 728950 chr6:70926588:G>A COL9A1 NM_078485:c.*12C>T THREE_PRIME_EXON Unknown significance rs778177942 This variant is a VUS because it does not have enough information. 0 10246 0 1 11470 8.7184e-05 0 8554 0 0 6566 0 2 66028 3.02902e-05 0 896 0 0 16374 0 3 120134 2.49721e-05 728951 chr6:70926605:G>A COL9A1 NM_078485:p.Pro678Ser NM_078485:c.2032C>T EXON32 Likely benign rs374561398 Pathogenicity is based on prediction data only. 2 out of 6 predictions were pathogenic. 0.045 N 0.0 D 0.005;0.008;0.005 B 0.141834 N 1 N;N;N 2.03 C 0 8600 0 1 4406 0.000226963 1 13006 7.68876e-05 1 10282 9.72573e-05 0 11522 0 1 8572 0.000116659 0 6590 0 0 66240 0 0 902 0 0 16448 0 2 120556 1.65898e-05 728952 chr6:70926605:G>T COL9A1 NM_078485:p.Pro678Thr NM_078485:c.2032C>A EXON32 Likely benign rs374561398 Pathogenicity is based on prediction data only. 2 out of 6 predictions were pathogenic. 0.045 N 0.0 D 0.023;0.039;0.023 B 0.141834 N 1 N;N;N 2.03 C 1 10282 9.72573e-05 0 11522 0 0 8572 0 0 6590 0 0 66240 0 0 902 0 0 16448 0 1 120556 8.2949e-06 728953 chr6:70926612:C>T COL9A1 NM_078485:p.Gly675Gly NM_078485:c.2025G>A EXON32 Unknown significance rs373430094 This variant is a VUS because it does not have enough information. 0 8600 0 1 4406 0.000226963 1 13006 7.68876e-05 4 10284 0.000388954 0 11534 0 0 8588 0 0 6594 0 0 66280 0 0 902 0 0 16472 0 4 120654 3.31527e-05 728954 chr6:70926613:C>T COL9A1 NM_078485:p.Gly675Glu NM_078485:c.2024G>A EXON32 Unknown significance rs370064762 This variant is a VUS because it does not have enough information. 0.892 N 0.0 D 1.0 D 0 D 0.997299 D;D;D 5.87 C 0 8600 0 1 4406 0.000226963 1 13006 7.68876e-05 728955 chr6:70926625:G>C COL9A1 NM_078485:p.Ala671Gly NM_078485:c.2012C>G EXON32 Unknown significance rs745872166 This variant is a VUS because it does not have enough information. 0.108 N 0.2;0.211 T 0.983;0.995;0.997 D 0.006579 N 0.977101 D;D;D 5.0 C 0 10286 0 0 11548 0 0 8598 0 0 6596 0 0 66328 0 0 900 0 1 16488 6.06502e-05 1 120744 8.28199e-06 728956 chr6:70926629:G>A COL9A1 NM_078485:p.Arg670Stop NM_078485:c.2008C>T EXON32 Unknown significance rs145221543 This variant is a VUS because it does not have enough information. 0.045 N 0.420448 N 1 D;D 4.98 C 0 8600 0 1 4406 0.000226963 1 13006 7.68876e-05 1 10276 9.73141e-05 0 11552 0 0 8602 0 0 6596 0 1 66336 1.50748e-05 0 902 0 0 16498 0 2 120762 1.65615e-05 728957 chr6:70926629:G>T COL9A1 NM_078485:p.Arg670Arg NM_078485:c.2008C>A EXON32 Unknown significance rs145221543 This variant is a VUS because it does not have enough information. 0 10276 0 0 11552 0 0 8602 0 0 6596 0 1 66336 1.50748e-05 0 902 0 0 16498 0 1 120762 8.28075e-06 728958 chr6:70926638:C>A COL9A1 NM_078485:p.Ala667Ser NM_078485:c.1999G>T EXON32 Unknown significance rs747451078 This variant is a VUS because it does not have enough information. -0.008 N 0.37;0.132 T 0.836;0.204;0.007 P;B;B 0.000107 N 0.992378 D;D;D 4.99 C 0 10282 0 0 11554 0 0 8608 0 0 6600 0 0 66326 0 0 904 0 1 16502 6.05987e-05 1 120776 8.27979e-06 728959 chr6:70926639:C>T COL9A1 NM_078485:p.Gln666Gln NM_078485:c.1998G>A EXON32 Unknown significance rs376876121 This variant is a VUS because it does not have enough information. 1 8600 0.000116279 0 4406 0 1 13006 7.68876e-05 0 10278 0 0 11556 0 0 8612 0 0 6600 0 1 66336 1.50748e-05 0 904 0 0 16502 0 1 120788 8.27897e-06 728960 chr6:70926641:G>T COL9A1 NM_078485:p.Gln666Lys NM_078485:c.1996C>A EXON32 Unknown significance rs772906014 This variant is a VUS because it does not have enough information. 0.998 C 0.024;0.015 D 0.997;0.977;0.969 D 1e-06 D 0.999784 D;D;D 5.87 C 0 10266 0 0 11556 0 0 8610 0 0 6600 0 1 66328 1.50766e-05 0 904 0 0 16500 0 1 120764 8.28061e-06 728961 chr6:70926645:G>A COL9A1 NM_078485:p.Thr664Thr NM_078485:c.1992C>T EXON32 Unknown significance rs567606245 This variant is a VUS because it does not have enough information. 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 0 10274 0 0 11558 0 0 8612 0 0 6600 0 3 66322 4.52339e-05 0 904 0 0 16502 0 3 120772 2.48402e-05 728962 chr6:70926659:G>C COL9A1 NM_078485:p.Pro660Ala NM_078485:c.1978C>G EXON32 Unknown significance rs764914222 This variant is a VUS because it does not have enough information. 0.998 C 0.457;0.014 T;D 0.88;0.945;0.477 P 1e-06 D 0.999743 D;D;D 5.87 C 728963 chr6:70926671:C>T COL9A1 NM_078485:p.Gly656Ser NM_078485:c.1966G>A EXON32 Unknown significance rs770502831 This variant is a VUS because it does not have enough information. 0.892 N 0.0;0.036 D 1.0 D 0 D 0.999999 D;D;D 5.87 C 0 10256 0 0 11558 0 0 8614 0 1 6598 0.000151561 0 66278 0 0 904 0 0 16508 0 1 120716 8.28391e-06 728964 chr6:70926672:G>A COL9A1 NM_078485:p.Pro655Pro NM_078485:c.1965C>T EXON32 Unknown significance rs370324739 This variant is a VUS because it does not have enough information. 0 8600 0 1 4406 0.000226963 1 13006 7.68876e-05 728965 chr6:70926677:G>A COL9A1 NM_078485:p.Leu654Phe NM_078485:c.1960C>T EXON32 Unknown significance rs773938837 This variant is a VUS because it does not have enough information. 0.998 C 0.176;0.062 T 0.997;0.991;0.56 D;D;P 0.00452 N 0.937461 D;D;D 5.87 C 0 10254 0 0 11558 0 0 8614 0 0 6598 0 1 66234 1.5098e-05 0 904 0 0 16510 0 1 120672 8.28693e-06 728966 chr6:70926682:G>C COL9A1 NM_078485:p.Pro652Arg NM_078485:c.1955C>G EXON32 Unknown significance rs758916884 This variant is a VUS because it does not have enough information. 0.998 C 0.953;0.328 T 0.992;0.985;0.782 D;D;P 0.014857 N 0.999975 D;D;D 5.87 C 0 10208 0 0 11554 0 1 8608 0.000116171 0 6592 0 0 66154 0 0 904 0 0 16510 0 1 120530 8.29669e-06 728967 chr6:70926689:C>T COL9A1 NM_078485:p.Gly650Arg NM_078485:c.1948G>A EXON32 Unknown significance rs767536535 This variant is a VUS because it does not have enough information. 0.892 N 0.0 D 1.0 D 0 D 1 D;D;D 5.87 C 0 10198 0 0 11550 0 0 8612 0 0 6592 0 0 66114 0 0 904 0 1 16510 6.05694e-05 1 120480 8.30013e-06 728968 chr6:70926690:C>T COL9A1 NM_078485:p.Pro649Pro NM_078485:c.1947G>A EXON32 Unknown significance rs199845159 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681 0 10194 0 0 11552 0 1 8608 0.000116171 0 6592 0 0 66074 0 0 902 0 0 16508 0 1 120430 8.30358e-06 728969 chr6:70926691:G>A COL9A1 NM_078485:p.Pro649Leu NM_078485:c.1946C>T EXON32 Unknown significance rs760617713 This variant is a VUS because it does not have enough information. 0.998 C 0.012;0.006 D 1.0 D 0 D 1 D;D;D 5.87 C 0 10190 0 0 11552 0 1 8608 0.000116171 0 6590 0 1 66080 1.51332e-05 0 902 0 0 16508 0 2 120430 1.66072e-05 728970 chr6:70926695:G>A COL9A1 NM_078485:p.Pro648Ser NM_078485:c.1942C>T EXON32 Unknown significance rs763970167 This variant is a VUS because it does not have enough information. 0.998 C 0.059;0.08 T 1.0 D 0 D 1 D;D;D 5.87 C 0 10184 0 0 11554 0 0 8610 0 0 6586 0 1 66096 1.51295e-05 0 902 0 0 16510 0 1 120442 8.30275e-06 728971 chr6:70926695:G>T COL9A1 NM_078485:p.Pro648Thr NM_078485:c.1942C>A EXON32 Unknown significance rs763970167 This variant is a VUS because it does not have enough information. 0.998 C 0.021;0.044 D 1.0 D 0 D 1 D;D;D 5.87 C 0 10184 0 0 11554 0 1 8610 0.000116144 0 6586 0 0 66096 0 0 902 0 0 16510 0 1 120442 8.30275e-06 728972 chr6:70926697:C>A COL9A1 NM_078485:p.Gly647Val NM_078485:c.1940G>T EXON32 Unknown significance rs757561926 This variant is a VUS because it does not have enough information. 0.892 N 0.0 D 1.0 D 0 D 1 D;D;D 5.87 C 0 10164 0 0 11552 0 0 8606 0 0 6586 0 1 66028 1.51451e-05 0 902 0 0 16510 0 1 120348 8.30924e-06 728973 chr6:70926722:C>G COL9A1 NM_078485:p.Val639Leu NM_078485:c.1915G>C EXON32 Likely benign rs1056923 Pathogenicity is based on prediction data only. 2 out of 6 predictions were pathogenic. 0.042 N 0.402;0.626 T 0.888;0.798;0.296 P;P;B 0.006532 N 0.999953 N;N;N 1.79 C 728974 chr6:70926722:C>T COL9A1 NM_078485:p.Val639Met NM_078485:c.1915G>A EXON32 Likely benign rs1056923 Pathogenicity is based on prediction data only. 2 out of 6 predictions were pathogenic. 0.042 N 0.125;0.065 T 0.999;0.993;0.957 D 0.006532 N 0.999945 N;N;N 1.79 C 0 10068 0 0 11544 0 1 8598 0.000116306 0 6586 0 0 65780 0 0 900 0 0 16504 0 1 119980 8.33472e-06 728975 chr6:70926729:G>A COL9A1 NM_078485:p.Pro636Pro NM_078485:c.1908C>T EXON32 Unknown significance rs750538159 This variant is a VUS because it does not have enough information. 0 10018 0 0 11540 0 0 8588 0 0 6586 0 3 65696 4.56649e-05 0 896 0 0 16502 0 3 119826 2.50363e-05 728976 chr6:70926737:G>C COL9A1 NM_078485:p.Arg634Gly NM_078485:c.1900C>G EXON32 Unknown significance rs758388716 This variant is a VUS because it does not have enough information. 0.998 C 0.014;0.087 D;T 0.995;0.98;0.351 D;D;B 6.5e-05 D 0.586536 N;N;N 4.98 C 0 9960 0 0 11534 0 0 8584 0 0 6580 0 0 65528 0 0 894 0 2 16498 0.000121227 2 119578 1.67255e-05 728977 chr6:70926743:C>T COL9A1 NM_078485:p.Gly632Ser NM_078485:c.1894G>A EXON32 Unknown significance rs199581593 This variant is a VUS because it does not have enough information. 0.892 N 0.0 D 1.0 D 0 D 1 D;D;D 5.87 C 0 9904 0 0 11526 0 0 8578 0 1 6580 0.000151976 4 65342 6.12164e-05 0 898 0 1 16496 6.06208e-05 6 119324 5.02833e-05 728978 chr6:70926744:G>A COL9A1 NM_078485:p.Asp631Asp NM_078485:c.1893C>T EXON32 Unknown significance rs149139869 This variant is a VUS because it does not have enough information. 3 8600 0.000348837 0 4406 0 3 13006 0.000230663 0 9902 0 0 11526 0 2 8582 0.000233046 0 6580 0 6 65338 9.18302e-05 0 898 0 0 16496 0 8 119322 6.70455e-05 728979 chr6:70926744:G>C COL9A1 NM_078485:p.Asp631Glu NM_078485:c.1893C>G EXON32 Unknown significance rs149139869 This variant is a VUS because it does not have enough information. -1.648 N 0.165;0.015 T;D 1.0;1.0;0.999 D 0 D 0.999187 D;D;D -3.09 N 0 9902 0 0 11526 0 1 8582 0.000116523 0 6580 0 0 65338 0 0 898 0 0 16496 0 1 119322 8.38068e-06 728980 chr6:70926748:C>A COL9A1 NM_078485:p.Arg630Leu NM_078485:c.1889G>T EXON32 Unknown significance rs201520437 This variant is a VUS because it does not have enough information. -1.007 N 0.007;0.244 D;T 0.999;0.998;0.999 D 0 D 0.999977 D;D;D 3.18 C 0 9878 0 0 11522 0 0 8580 0 0 6578 0 3 65320 4.59277e-05 0 898 0 0 16494 0 3 119270 2.5153e-05 728981 chr6:70926748:C>T COL9A1 NM_078485:p.Arg630Gln NM_078485:c.1889G>A EXON32 Unknown significance rs201520437 This variant is a VUS because it does not have enough information. -1.007 N 0.092;0.205 T 0.986;0.983;0.999 D 0 D 0.999826 D;D;D 3.18 C 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681 0 9878 0 0 11522 0 0 8580 0 0 6578 0 1 65320 1.53092e-05 0 898 0 0 16494 0 1 119270 8.38434e-06 728982 chr6:70926749:G>C COL9A1 NM_078485:p.Arg630Gly NM_078485:c.1888C>G EXON32 Unknown significance rs200829297 This variant is a VUS because it does not have enough information. 0.998 C 0.005;0.068 D;T 1.0;0.998;0.999 D 0 D 0.999978 D;D;D 5.87 C 2 8600 0.000232558 0 4406 0 2 13006 0.000153775 0 9876 0 0 11522 0 0 8576 0 0 6576 0 2 65278 3.06382e-05 0 898 0 0 16494 0 2 119220 1.67757e-05 728983 chr6:70926753:A>G COL9A1 NM_078485:p.Asn628Asn NM_078485:c.1884T>C EXON32 Unknown significance rs773848465 This variant is a VUS because it does not have enough information. 0 9846 0 7 11518 0.000607744 0 8578 0 0 6576 0 0 65234 0 0 898 0 0 16494 0 7 119144 5.87524e-05 728984 chr6:70926757:C>T COL9A1 NM_078485:p.Arg627Lys NM_078485:c.1880G>A EXON32 Likely benign rs1056921 Pathogenicity is based on prediction data only. 1 out of 6 predictions were pathogenic. 0.049 N 0.937;0.4 T 0.092;0.007;0.0 B 0.000433 N 0.614331 N;N;N 2.67 C 728985 chr6:70926759:G>C COL9A1 NM_078485:p.Gly626Gly NM_078485:c.1878C>G EXON32 Unknown significance rs1056920 This variant is a VUS because it does not have enough information. 728986 chr6:70926776:C>G COL9A1 NM_078485:p.Gly621Arg NM_078485:c.1861G>C EXON32 Unknown significance rs745421286 This variant is a VUS because it does not have enough information. 0.892 N 0.0 D 1.0 D 0 D 1 D;D;D 4.75 C 0 9622 0 1 11492 8.70171e-05 0 8550 0 0 6558 0 0 64734 0 0 886 0 0 16472 0 1 118314 8.45209e-06 728987 chr6:70926778:G>A COL9A1 NM_078485:p.Pro620Leu NM_078485:c.1859C>T EXON32 Unknown significance rs569046385 This variant is a VUS because it does not have enough information. 0.108 N 0.045;0.009 D 1.0 D 2.6e-05 D 1 D;D;D 4.76 C 728988 chr6:70926781:T>G COL9A1 NM_078485:p.Asp619Ala NM_078485:c.1856A>C EXON32 Unknown significance rs202176764 This variant is a VUS because it does not have enough information. 1.011 C 0.229;0.085 T 0.881;0.666;0.124 P;P;B 1e-06 D 0.998343 D;D;D 5.63 C 9 8596 0.001047 0 4406 0 9 13002 0.000692201 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 0 9612 0 0 11484 0 0 8552 0 0 6552 0 43 64704 0.000664565 0 886 0 0 16468 0 43 118258 0.000363612 728989 chr6:70926786:T>C COL9A1 NM_078485:c.1853-2A>G INTRON31 Unknown significance rs775559838 This variant is a VUS because it does not have enough information. 1.011 C 1 D 5.63 C 0 9560 0 0 11476 0 0 8548 0 0 6548 0 0 64610 0 0 886 0 1 16464 6.07386e-05 1 118092 8.46797e-06 728990 chr6:70926787:G>A COL9A1 NM_078485:c.1853-3C>T INTRON31 Unknown significance rs760704462 This variant is a VUS because it does not have enough information. 0 9528 0 1 11474 8.71536e-05 0 8544 0 0 6548 0 1 64530 1.54967e-05 0 882 0 0 16458 0 2 117964 1.69543e-05 728991 chr6:70926790:AC>- COL9A1 NM_078485:c.1853-6_1853-3delGT INTRON31 Unknown significance rs773034538 This variant is a VUS because it does not have enough information. 0 9538 0 0 11476 0 0 8544 0 0 6548 0 6 64526 9.29858e-05 0 882 0 0 16460 0 6 117974 5.08587e-05 728992 chr6:70926799:A>G COL9A1 NM_078485:c.1853-15T>C INTRON31 Unknown significance rs764060012 This variant is a VUS because it does not have enough information. 0 9488 0 0 11466 0 0 8542 0 0 6548 0 0 64326 0 0 880 0 1 16442 6.08199e-05 1 117692 8.49675e-06 728993 chr6:70926805:C>T COL9A1 NM_078485:c.1853-21G>A INTRON31 Unknown significance rs776603064 This variant is a VUS because it does not have enough information. 0 9440 0 0 11446 0 0 8532 0 0 6526 0 1 64196 1.55773e-05 0 876 0 0 16434 0 1 117450 8.51426e-06 728994 chr6:70926807:C>T COL9A1 NM_078485:c.1853-23G>A INTRON31 Unknown significance rs761652460 This variant is a VUS because it does not have enough information. 0 9446 0 0 11442 0 0 8530 0 0 6532 0 1 64200 1.55763e-05 0 876 0 1 16430 6.08643e-05 2 117456 1.70277e-05 728995 chr6:70926819:A>G COL9A1 NM_078485:c.1853-35T>C INTRON31 Unknown significance rs765545489 This variant is a VUS because it does not have enough information. 0 9414 0 0 11418 0 2 8504 0.000235183 0 6516 0 0 64008 0 0 876 0 0 16414 0 2 117150 1.70721e-05 728996 chr6:70926821:A>G COL9A1 NM_078485:c.1853-37T>C INTRON31 Unknown significance rs750581928 This variant is a VUS because it does not have enough information. 0 9394 0 0 11404 0 0 8498 0 0 6500 0 1 63972 1.56318e-05 0 874 0 0 16412 0 1 117054 8.54307e-06 728997 chr6:70926823:T>C COL9A1 NM_078485:c.1853-39A>G INTRON31 Unknown significance rs372462643 This variant is a VUS because it does not have enough information. 0 8590 0 1 4398 0.000227376 1 12988 7.69941e-05 728998 chr6:70926824:C>A COL9A1 NM_078485:c.1853-40G>T INTRON31 Unknown significance rs200640478 This variant is a VUS because it does not have enough information. 19 8590 0.00221187 1 4398 0.000227376 20 12988 0.00153988 0 1322 0 2 1006 0.002 1 694 0.0014 0 1008 0 1 978 0.001 4 5008 0.000798722 1 9388 0.000106519 25 11402 0.0021926 0 8488 0 1 6496 0.000153941 116 63898 0.00181539 2 876 0.00228311 55 16410 0.00335161 200 116958 0.00171002 728999 chr6:70926829:T>C COL9A1 NM_078485:c.1853-45A>G INTRON31 Unknown significance rs370148201 This variant is a VUS because it does not have enough information. 1 8584 0.000116496 0 4398 0 1 12982 7.70297e-05 0 9360 0 0 11392 0 0 8476 0 0 6494 0 6 63824 9.40085e-05 0 876 0 1 16396 6.09905e-05 7 116818 5.99223e-05 729000 chr6:70926835:C>T COL9A1 NM_078485:c.1853-51G>A INTRON31 Unknown significance rs373065340 This variant is a VUS because it does not have enough information. 1 8582 0.000116523 0 4396 0 1 12978 7.70535e-05 0 9298 0 0 11336 0 0 8438 0 0 6446 0 1 63550 1.57356e-05 0 868 0 0 16358 0 1 116294 8.5989e-06 729001 chr6:70926854:G>A COL9A1 NM_078485:c.1853-70C>T INTRON31 Unknown significance rs554434490 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 729002 chr6:70926863:C>T COL9A1 NM_078485:c.1853-79G>A INTRON31 Unknown significance rs574305278 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 729003 chr6:70926887:C>T COL9A1 NM_078485:c.1853-103G>A INTRON31 Benign rs9455004 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 79 1322 0.0598 1 1006 0.001 4 694 0.0058 0 1008 0 0 978 0 84 5008 0.0167732 729004 chr6:70926888:G>A COL9A1 NM_078485:c.1853-104C>T INTRON31 Unknown significance rs778257967 This variant is a VUS because it does not have enough information. 729005 chr6:70926898:G>A COL9A1 NM_078485:c.1853-114C>T INTRON31 Benign rs1200569 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 1124 1322 0.8502 733 1006 0.7286 597 694 0.8602 829 1008 0.8224 734 978 0.7505 4017 5008 0.802117 729006 chr6:70926933:G>C COL9A1 NM_078485:c.1853-149C>G INTRON31 Benign rs2881343 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 374 1322 0.2829 156 1006 0.1551 149 694 0.2147 98 1008 0.0972 255 978 0.2607 1032 5008 0.20607 729007 chr6:70926941:T>C COL9A1 NM_078485:c.1853-157A>G INTRON31 Unknown significance rs750731160 This variant is a VUS because it does not have enough information. 729008 chr6:70926948:A>G COL9A1 NM_078485:c.1853-164T>C INTRON31 Benign rs9455005 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 79 1322 0.0598 1 1006 0.001 4 694 0.0058 1 1008 0.001 0 978 0 85 5008 0.0169728 729009 chr6:70926955:T>C COL9A1 NM_078485:c.1853-171A>G INTRON31 Unknown significance rs565025254 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681 729010 chr6:70926979:A>G COL9A1 NM_078485:c.1853-195T>C INTRON31 Unknown significance rs116353596 This variant is a VUS because it does not have enough information. 6 1322 0.0045 0 1006 0 0 694 0 0 1008 0 0 978 0 6 5008 0.00119808 729011 chr6:70927015:T>A COL9A1 NM_078485:c.1853-231A>T INTRON31 Benign rs77849671 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 36 1322 0.0272 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 38 5008 0.00758786 729012 chr6:70927022:C>T COL9A1 NM_078485:c.1853-238G>A INTRON31 Unknown significance rs753964715 This variant is a VUS because it does not have enough information. 729013 chr6:70927042:C>T COL9A1 NM_078485:c.1853-258G>A INTRON31 Benign rs182674097 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 17 1322 0.0129 0 1006 0 0 694 0 0 1008 0 0 978 0 17 5008 0.00339457 729014 chr6:70927127:A>C COL9A1 NM_078485:c.1853-343T>G INTRON31 Unknown significance rs570598744 This variant is a VUS because it does not have enough information. 4 1322 0.003 0 1006 0 0 694 0 0 1008 0 0 978 0 4 5008 0.000798722 729015 chr6:70927152:G>C COL9A1 NM_078485:c.1853-368C>G INTRON31 Benign rs662828 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 461 1322 0.3487 300 1006 0.2982 322 694 0.464 444 1008 0.4405 257 978 0.2628 1784 5008 0.35623 729016 chr6:70927154:T>C COL9A1 NM_078485:c.1853-370A>G INTRON31 Unknown significance rs546784496 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 729017 chr6:70927185:T>G COL9A1 NM_078485:c.1853-401A>C INTRON31 Unknown significance rs746988967 This variant is a VUS because it does not have enough information. 729018 chr6:70927220:C>T COL9A1 NM_078485:c.1853-436G>A INTRON31 Unknown significance rs770715612 This variant is a VUS because it does not have enough information. 729019 chr6:70927268:T>A COL9A1 NM_078485:c.1853-484A>T INTRON31 Unknown significance rs112749797 This variant is a VUS because it does not have enough information. 729020 chr6:70927290:G>T COL9A1 NM_078485:c.1853-506C>A INTRON31 Unknown significance rs377694621 This variant is a VUS because it does not have enough information. 729021 chr6:70927312:A>G COL9A1 NM_078485:c.1853-528T>C INTRON31 Unknown significance rs558058201 This variant is a VUS because it does not have enough information. 0 1322 0 1 1006 0.001 2 694 0.0029 0 1008 0 1 978 0.001 4 5008 0.000798722 729022 chr6:70927330:G>A COL9A1 NM_078485:c.1853-546C>T INTRON31 Benign rs9455006 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 79 1322 0.0598 1 1006 0.001 4 694 0.0058 0 1008 0 0 978 0 84 5008 0.0167732 729023 chr6:70927331:C>A COL9A1 NM_078485:c.1853-547G>T INTRON31 Unknown significance rs568856737 This variant is a VUS because it does not have enough information. 729024 chr6:70927333:C>T COL9A1 NM_078485:c.1853-549G>A INTRON31 Unknown significance rs571945044 This variant is a VUS because it does not have enough information. 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 729025 chr6:70927384:T>C COL9A1 NM_078485:c.1853-600A>G INTRON31 Unknown significance rs534467225 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681 729026 chr6:70927392:C>T COL9A1 NM_078485:c.1853-608G>A INTRON31 Unknown significance rs576424152 This variant is a VUS because it does not have enough information. 729027 chr6:70927397:G>A COL9A1 NM_078485:c.1853-613C>T INTRON31 Unknown significance rs543603395 This variant is a VUS because it does not have enough information. 729028 chr6:70927415:T>C COL9A1 NM_078485:c.1853-631A>G INTRON31 Unknown significance rs150392551 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361 729029 chr6:70927425:A>C COL9A1 NM_078485:c.1853-641T>G INTRON31 Unknown significance rs769333464 This variant is a VUS because it does not have enough information. 729030 chr6:70927434:G>A COL9A1 NM_078485:c.1853-650C>T INTRON31 Benign rs661521 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 288 1322 0.2179 47 1006 0.0467 27 694 0.0389 7 1008 0.0069 61 978 0.0624 430 5008 0.0858626 729031 chr6:70927508:T>A COL9A1 NM_078485:c.1853-724A>T INTRON31 Benign rs1200568 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 386 1322 0.292 299 1006 0.2972 318 694 0.4582 444 1008 0.4405 257 978 0.2628 1704 5008 0.340256 729032 chr6:70927523:C>T COL9A1 NM_078485:c.1853-739G>A INTRON31 Unknown significance rs762410593 This variant is a VUS because it does not have enough information. 729033 chr6:70927531:T>C COL9A1 NM_078485:c.1853-747A>G INTRON31 Unknown significance rs556380808 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361 729034 chr6:70927666:->A COL9A1 NM_078485:c.1853-882_1853-881insT INTRON31 Unknown significance rs541153953 This variant is a VUS because it does not have enough information. 729035 chr6:70927672:C>T COL9A1 NM_078485:c.1853-888G>A INTRON31 Unknown significance rs768672054 This variant is a VUS because it does not have enough information. 729036 chr6:70927687:T>C COL9A1 NM_078485:c.1853-903A>G INTRON31 Unknown significance rs576521971 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 729037 chr6:70927752:A>G COL9A1 NM_078485:c.1853-968T>C INTRON31 Unknown significance rs545059587 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681 729038 chr6:70927754:G>A COL9A1 NM_078485:c.1853-970C>T INTRON31 Benign rs138158570 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 45 1322 0.034 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 46 5008 0.0091853 729039 chr6:70927771:G>A COL9A1 NM_078485:c.1853-987C>T INTRON31 Unknown significance rs761675420 This variant is a VUS because it does not have enough information. 729040 chr6:70927789:T>C COL9A1 NM_078485:c.1853-1005A>G INTRON31 Benign rs142404885 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 31 1322 0.0234 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 33 5008 0.00658946 729041 chr6:70927825:G>A COL9A1 NM_078485:c.1853-1041C>T INTRON31 Unknown significance rs540895476 This variant is a VUS because it does not have enough information. 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 729042 chr6:70927840:C>T COL9A1 NM_078485:c.1853-1056G>A INTRON31 Unknown significance rs779580023 This variant is a VUS because it does not have enough information. 729043 chr6:70927841:G>C COL9A1 NM_078485:c.1853-1057C>G INTRON31 Unknown significance rs560859980 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681 729044 chr6:70927844:T>A COL9A1 NM_078485:c.1853-1060A>T INTRON31 Unknown significance rs763042157 This variant is a VUS because it does not have enough information. 729045 chr6:70927849:->AAT COL9A1 NM_078485:c.1853-1065_1853-1064insATT INTRON31 Benign rs557920792 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 8 1322 0.0061 0 1006 0 0 694 0 0 1008 0 1 978 0.001 9 5008 0.00179712 729046 chr6:70927881:C>T COL9A1 NM_078485:c.1853-1097G>A INTRON31 Unknown significance rs773688963 This variant is a VUS because it does not have enough information. 729047 chr6:70927886:G>A COL9A1 NM_078485:c.1853-1102C>T INTRON31 Unknown significance rs184914476 This variant is a VUS because it does not have enough information. 0 1322 0 2 1006 0.002 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361 729048 chr6:70927904:T>C COL9A1 NM_078485:c.1853-1120A>G INTRON31 Unknown significance rs767948610 This variant is a VUS because it does not have enough information. 729049 chr6:70927910:T>C COL9A1 NM_078485:c.1853-1126A>G INTRON31 Unknown significance rs146611546 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681 729050 chr6:70927937:T>C COL9A1 NM_078485:c.1853-1153A>G INTRON31 Unknown significance rs563219814 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 729051 chr6:70927944:G>C COL9A1 NM_078485:c.1853-1160C>G INTRON31 Unknown significance rs532911506 This variant is a VUS because it does not have enough information. 729052 chr6:70927967:T>A COL9A1 NM_078485:c.1853-1183A>T INTRON31 Benign rs476863 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 460 1322 0.348 300 1006 0.2982 322 694 0.464 444 1008 0.4405 257 978 0.2628 1783 5008 0.35603 729053 chr6:70927975:T>C COL9A1 NM_078485:c.1853-1191A>G INTRON31 Unknown significance rs552007772 This variant is a VUS because it does not have enough information. 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 729054 chr6:70928002:A>G COL9A1 NM_078485:c.1853-1218T>C INTRON31 Unknown significance rs565644726 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681 729055 chr6:70928009:T>G COL9A1 NM_078485:c.1853-1225A>C INTRON31 Unknown significance rs528101602 This variant is a VUS because it does not have enough information. 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 729056 chr6:70928032:G>A COL9A1 NM_078485:c.1853-1248C>T INTRON31 Unknown significance rs548062553 This variant is a VUS because it does not have enough information. 1 1322 0.0008 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 2 5008 0.000399361 729057 chr6:70928042:G>T COL9A1 NM_078485:c.1853-1258C>A INTRON31 Unknown significance rs766625505 This variant is a VUS because it does not have enough information. 729058 chr6:70928046:G>A COL9A1 NM_078485:c.1853-1262C>T INTRON31 Unknown significance rs754117076 This variant is a VUS because it does not have enough information. 729059 chr6:70928060:G>A COL9A1 NM_078485:c.1853-1276C>T INTRON31 Unknown significance rs755105909 This variant is a VUS because it does not have enough information. 729060 chr6:70928077:G>A COL9A1 NM_078485:c.1853-1293C>T INTRON31 Unknown significance rs568008085 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681 729061 chr6:70928089:G>A COL9A1 NM_078485:c.1853-1305C>T INTRON31 Benign rs370453291 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 0 1322 0 0 1006 0 0 694 0 0 1008 0 15 978 0.0153 15 5008 0.00299521 729062 chr6:70928091:G>A COL9A1 NM_078485:c.1853-1307C>T INTRON31 Unknown significance rs189729053 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681 729063 chr6:70928114:C>T COL9A1 NM_078485:c.1853-1330G>A INTRON31 Unknown significance rs779062530 This variant is a VUS because it does not have enough information. 729064 chr6:70928152:C>T COL9A1 NM_078485:c.1853-1368G>A INTRON31 Unknown significance rs570029367 This variant is a VUS because it does not have enough information. 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 729065 chr6:70928195:G>C COL9A1 NM_078485:c.1853-1411C>G INTRON31 Unknown significance rs759738915 This variant is a VUS because it does not have enough information. 729066 chr6:70928251:T>C COL9A1 NM_078485:c.1853-1467A>G INTRON31 Unknown significance rs757284588 This variant is a VUS because it does not have enough information. 729067 chr6:70928322:T>C COL9A1 NM_078485:c.1853-1538A>G INTRON31 Unknown significance rs183148585 This variant is a VUS because it does not have enough information. 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 729068 chr6:70928334:T>C COL9A1 NM_078485:c.1853-1550A>G INTRON31 Benign rs72918976 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 2 1322 0.0015 9 1006 0.0089 2 694 0.0029 0 1008 0 3 978 0.0031 16 5008 0.00319489 729069 chr6:70928337:G>T COL9A1 NM_078485:c.1853-1553C>A INTRON31 Unknown significance rs189118219 This variant is a VUS because it does not have enough information. 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 729070 chr6:70928359:T>C COL9A1 NM_078485:c.1853-1575A>G INTRON31 Unknown significance rs758506278 This variant is a VUS because it does not have enough information. 729071 chr6:70928368:CTTTT>- COL9A1 NM_078485:c.1853-1584_1853-1578delAAAAG INTRON31 Unknown significance rs372428882 This variant is a VUS because it does not have enough information. 729072 chr6:70928371:T>C COL9A1 NM_078485:c.1853-1587A>G INTRON31 Benign rs541032331 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 8 1322 0.0061 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 9 5008 0.00179712 729073 chr6:70928392:C>- COL9A1 NM_078485:c.1853-1608delG INTRON31 Unknown significance rs373177713 This variant is a VUS because it does not have enough information. 729074 chr6:70928392:C>T COL9A1 NM_078485:c.1853-1608G>A INTRON31 Benign rs12201251 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 75 1322 0.0567 252 1006 0.2505 291 694 0.4193 437 1008 0.4335 196 978 0.2004 1251 5008 0.2498 729075 chr6:70928398:A>T COL9A1 NM_078485:c.1853-1614T>A INTRON31 Unknown significance rs778205161 This variant is a VUS because it does not have enough information. 729076 chr6:70928400:A>T COL9A1 NM_078485:c.1853-1616T>A INTRON31 Unknown significance rs752112221 This variant is a VUS because it does not have enough information. 729077 chr6:70928402:G>T COL9A1 NM_078485:c.1853-1618C>A INTRON31 Unknown significance rs757612482 This variant is a VUS because it does not have enough information. 729078 chr6:70928404:C>T COL9A1 NM_078485:c.1853-1620G>A INTRON31 Unknown significance rs781466206 This variant is a VUS because it does not have enough information. 729079 chr6:70928431:G>T COL9A1 NM_078485:c.1853-1647C>A INTRON31 Unknown significance rs549163102 This variant is a VUS because it does not have enough information. 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 729080 chr6:70928441:->AGTGGTCTT COL9A1 NM_078485:c.1853-1657_1853-1656insAAGACCACT INTRON31 Unknown significance rs202152808 This variant is a VUS because it does not have enough information. 729081 chr6:70928441:->AGTGGTCTTATT COL9A1 NM_078485:c.1853-1657_1853-1656insAATAAGACCACT INTRON31 Unknown significance rs202152808 This variant is a VUS because it does not have enough information. 729082 chr6:70928442:->G COL9A1 NM_078485:c.1853-1658_1853-1657insC INTRON31 Unknown significance rs765711033 This variant is a VUS because it does not have enough information. 729083 chr6:70928442:T>C COL9A1 NM_078485:c.1853-1658A>G INTRON31 Unknown significance rs16868762 This variant is a VUS because it does not have enough information. 729085 chr6:70928443:->AGGTCTTATTAC COL9A1 NM_078485:c.1853-1659_1853-1658insGTAATAAGACCT INTRON31 Unknown significance rs3842608 This variant is a VUS because it does not have enough information. 729086 chr6:70928443:->GGTCTTATTAC COL9A1 NM_078485:c.1853-1659_1853-1658insGTAATAAGACC INTRON31 Unknown significance rs66525752 This variant is a VUS because it does not have enough information. 729084 chr6:70928443:->GTGGTCTTATTAC COL9A1 NM_078485:c.1853-1659_1853-1658insGTAATAAGACCAC INTRON31 Unknown significance rs369801517 This variant is a VUS because it does not have enough information. 729087 chr6:70928443:->TGGTCTTATTAC COL9A1 NM_078485:c.1853-1659_1853-1658insGTAATAAGACCA INTRON31 Unknown significance rs66525752 This variant is a VUS because it does not have enough information. 729088 chr6:70928505:T>C COL9A1 NM_078485:c.1853-1721A>G INTRON31 Benign rs491690 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 300 1322 0.2269 0 1006 0 13 694 0.0187 0 1008 0 0 978 0 313 5008 0.0625 729089 chr6:70928505:TT>CA COL9A1 Unknown significance rs386702482 This variant is a VUS because it does not have enough information. 729090 chr6:70928506:T>A COL9A1 NM_078485:c.1853-1722A>T INTRON31 Benign rs75370620 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 98 1322 0.0741 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 99 5008 0.0197684 729091 chr6:70928528:C>G COL9A1 NM_078485:c.1853-1744G>C INTRON31 Unknown significance rs371962151 This variant is a VUS because it does not have enough information. 729092 chr6:70928600:A>G COL9A1 NM_078485:c.1853-1816T>C INTRON31 Benign rs12333183 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 50 1322 0.0378 1 1006 0.001 2 694 0.0029 0 1008 0 0 978 0 53 5008 0.0105831 729093 chr6:70928628:G>C COL9A1 NM_078485:c.1853-1844C>G INTRON31 Unknown significance rs567891451 This variant is a VUS because it does not have enough information. 729094 chr6:70928678:C>A COL9A1 NM_078485:c.1853-1894G>T INTRON31 Unknown significance rs768138513 This variant is a VUS because it does not have enough information. 729095 chr6:70928686:G>A COL9A1 NM_078485:c.1853-1902C>T INTRON31 Unknown significance rs545874453 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 0 694 0 0 1008 0 3 978 0.0031 3 5008 0.000599042 729096 chr6:70928699:C>G COL9A1 NM_078485:c.1853-1915G>C INTRON31 Unknown significance rs779784277 This variant is a VUS because it does not have enough information. 729097 chr6:70928708:T>C COL9A1 NM_078485:c.1853-1924A>G INTRON31 Unknown significance rs559493098 This variant is a VUS because it does not have enough information. 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 729098 chr6:70928816:A>G COL9A1 NM_078485:c.1853-2032T>C INTRON31 Unknown significance rs542932446 This variant is a VUS because it does not have enough information. 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361 729099 chr6:70928828:G>A COL9A1 NM_078485:c.1853-2044C>T INTRON31 Unknown significance rs548249586 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 729100 chr6:70928844:A>G COL9A1 NM_078485:c.1853-2060T>C INTRON31 Benign rs9346372 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 75 1322 0.0567 252 1006 0.2505 291 694 0.4193 438 1008 0.4345 196 978 0.2004 1252 5008 0.25 729101 chr6:70928882:C>T COL9A1 NM_078485:c.1853-2098G>A INTRON31 Unknown significance rs73749904 This variant is a VUS because it does not have enough information. 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 1 978 0.001 2 5008 0.000399361 729102 chr6:70928883:G>A COL9A1 NM_078485:c.1853-2099C>T INTRON31 Benign rs17691623 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 2 1322 0.0015 11 1006 0.0109 2 694 0.0029 14 1008 0.0139 0 978 0 29 5008 0.00579073 729103 chr6:70928914:C>A COL9A1 NM_078485:c.1853-2130G>T INTRON31 Benign rs487928 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 301 1322 0.2277 47 1006 0.0467 27 694 0.0389 7 1008 0.0069 61 978 0.0624 443 5008 0.0884585 729104 chr6:70928914:C>G COL9A1 NM_078485:c.1853-2130G>C INTRON31 Unknown significance rs487928 This variant is a VUS because it does not have enough information. 729105 chr6:70928998:G>- COL9A1 NM_078485:c.1853-2214delC INTRON31 Benign rs562620805 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 30 1322 0.0227 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 31 5008 0.0061901 729106 chr6:70929004:->A COL9A1 NM_078485:c.1853-2220_1853-2219insT INTRON31 Benign rs148826101 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 3 1322 0.0023 32 1006 0.0318 6 694 0.0086 0 1008 0 11 978 0.0112 52 5008 0.0103834 729107 chr6:70929017:G>A COL9A1 NM_078485:c.1853-2233C>T INTRON31 Unknown significance rs771982291 This variant is a VUS because it does not have enough information. 729108 chr6:70929020:A>T COL9A1 NM_078485:c.1853-2236T>A INTRON31 Unknown significance rs761127709 This variant is a VUS because it does not have enough information. 729109 chr6:70929071:G>A COL9A1 NM_078485:c.1853-2287C>T INTRON31 Unknown significance rs766748350 This variant is a VUS because it does not have enough information. 729110 chr6:70929088:C>G COL9A1 NM_078485:c.1853-2304G>C INTRON31 Unknown significance rs538871527 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681 729111 chr6:70929089:G>A COL9A1 NM_078485:c.1853-2305C>T INTRON31 Unknown significance rs754093013 This variant is a VUS because it does not have enough information. 729112 chr6:70929099:A>C COL9A1 NM_078485:c.1853-2315T>G INTRON31 Unknown significance rs552208407 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681 729113 chr6:70929132:G>A COL9A1 NM_078485:c.1853-2348C>T INTRON31 Unknown significance rs565884793 This variant is a VUS because it does not have enough information. 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 729114 chr6:70929138:G>A COL9A1 NM_078485:c.1853-2354C>T INTRON31 Unknown significance rs534681574 This variant is a VUS because it does not have enough information. 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 729115 chr6:70929167:C>T COL9A1 NM_078485:c.1853-2383G>A INTRON31 Unknown significance rs193135193 This variant is a VUS because it does not have enough information. 0 1322 0 2 1006 0.002 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361 729116 chr6:70929213:C>T COL9A1 NM_078485:c.1853-2429G>A INTRON31 Unknown significance rs765371389 This variant is a VUS because it does not have enough information. 729117 chr6:70929217:A>G COL9A1 NM_078485:c.1853-2433T>C INTRON31 Unknown significance rs183587563 This variant is a VUS because it does not have enough information. 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 729118 chr6:70929254:C>T COL9A1 NM_078485:c.1853-2470G>A INTRON31 Unknown significance rs200327588 This variant is a VUS because it does not have enough information. 729119 chr6:70929277:C>T COL9A1 NM_078485:c.1853-2493G>A INTRON31 Unknown significance rs537316187 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 729120 chr6:70929282:A>C COL9A1 NM_078485:c.1853-2498T>G INTRON31 Benign rs188572138 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 0 1322 0 5 1006 0.005 0 694 0 0 1008 0 1 978 0.001 6 5008 0.00119808 729121 chr6:70929292:C>G COL9A1 NM_078485:c.1853-2508G>C INTRON31 Unknown significance rs758531656 This variant is a VUS because it does not have enough information. 729122 chr6:70929296:G>C COL9A1 NM_078485:c.1853-2512C>G INTRON31 Unknown significance rs191756110 This variant is a VUS because it does not have enough information. 729123 chr6:70929296:G>T COL9A1 NM_078485:c.1853-2512C>A INTRON31 Unknown significance rs191756110 This variant is a VUS because it does not have enough information. 0 1322 0 1 1006 0.001 1 694 0.0014 0 1008 0 0 978 0 2 5008 0.000399361 729124 chr6:70929319:C>T COL9A1 NM_078485:c.1853-2535G>A INTRON31 Unknown significance rs184182028 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681 729125 chr6:70929327:T>C COL9A1 NM_078485:c.1853-2543A>G INTRON31 Unknown significance rs760527581 This variant is a VUS because it does not have enough information. 729126 chr6:70929334:G>T COL9A1 NM_078485:c.1853-2550C>A INTRON31 Unknown significance rs188166413 This variant is a VUS because it does not have enough information. 1 1322 0.0008 3 1006 0.003 2 694 0.0029 0 1008 0 1 978 0.001 7 5008 0.00139776 729127 chr6:70929368:G>A COL9A1 NM_078485:c.1853-2584C>T INTRON31 Unknown significance rs796160588 This variant is a VUS because it does not have enough information. 729128 chr6:70929369:A>C COL9A1 NM_078485:c.1853-2585T>G INTRON31 Unknown significance rs537381432 This variant is a VUS because it does not have enough information. 729129 chr6:70929411:C>T COL9A1 NM_078485:c.1853-2627G>A INTRON31 Benign rs35022420 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 367 1322 0.2776 101 1006 0.1004 136 694 0.196 96 1008 0.0952 222 978 0.227 922 5008 0.184105 729130 chr6:70929411:CA>TG COL9A1 Unknown significance rs386702483 This variant is a VUS because it does not have enough information. 729131 chr6:70929412:A>G COL9A1 NM_078485:c.1853-2628T>C INTRON31 Benign rs572716 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 1109 1322 0.8389 715 1006 0.7107 594 694 0.8559 713 1008 0.7073 675 978 0.6902 3806 5008 0.759984 729132 chr6:70929415:G>A COL9A1 NM_078485:c.1853-2631C>T INTRON31 Unknown significance rs561697786 This variant is a VUS because it does not have enough information. 0 1322 0 2 1006 0.002 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361 729133 chr6:70929463:G>T COL9A1 NM_078485:c.1853-2679C>A INTRON31 Unknown significance rs754729533 This variant is a VUS because it does not have enough information. 729134 chr6:70929470:A>- COL9A1 NM_078485:c.1853-2686delT INTRON31 Benign rs564251786 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 12 1322 0.0091 1 1006 0.001 0 694 0 0 1008 0 0 978 0 13 5008 0.00259585 729135 chr6:70929491:A>G COL9A1 NM_078485:c.1853-2707T>C INTRON31 Unknown significance rs778405664 This variant is a VUS because it does not have enough information. 729136 chr6:70929514:C>G COL9A1 NM_078485:c.1853-2730G>C INTRON31 Unknown significance rs747731798 This variant is a VUS because it does not have enough information. 729137 chr6:70929522:T>G COL9A1 NM_078485:c.1853-2738A>C INTRON31 Benign rs10806630 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 7 1322 0.0053 100 1006 0.0994 23 694 0.0331 33 1008 0.0327 100 978 0.1022 263 5008 0.052516 729138 chr6:70929526:A>T COL9A1 NM_078485:c.1853-2742T>A INTRON31 Unknown significance rs550412692 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 729139 chr6:70929527:T>- COL9A1 NM_078485:c.1853-2743delA INTRON31 Benign rs552997977 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 0 1322 0 7 1006 0.007 1 694 0.0014 0 1008 0 0 978 0 8 5008 0.00159744 729140 chr6:70929597:A>G COL9A1 NM_078485:c.1853-2813T>C INTRON31 Unknown significance rs546645983 This variant is a VUS because it does not have enough information. 729141 chr6:70929616:A>G COL9A1 NM_078485:c.1853-2832T>C INTRON31 Benign rs563832286 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 9 1322 0.0068 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 10 5008 0.00199681 729142 chr6:70929621:T>- COL9A1 NM_078485:c.1853-2837delA INTRON31 Unknown significance rs35130017 This variant is a VUS because it does not have enough information. 729143 chr6:70929715:C>A COL9A1 NM_078485:c.1853-2931G>T INTRON31 Unknown significance rs532738653 This variant is a VUS because it does not have enough information. 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 729144 chr6:70929758:C>T COL9A1 NM_078485:c.1853-2974G>A INTRON31 Unknown significance rs191479699 This variant is a VUS because it does not have enough information. 5 1322 0.0038 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 6 5008 0.00119808 729145 chr6:70929814:C>A COL9A1 NM_078485:c.1853-3030G>T INTRON31 Unknown significance rs747528454 This variant is a VUS because it does not have enough information. 729146 chr6:70929834:T>C COL9A1 NM_078485:c.1853-3050A>G INTRON31 Unknown significance rs752046906 This variant is a VUS because it does not have enough information. 729147 chr6:70929843:->TCA COL9A1 NM_078485:c.1853-3059_1853-3058insTGA INTRON31 Benign rs147934773 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 192 1322 0.1452 15 1006 0.0149 7 694 0.0101 121 1008 0.12 42 978 0.0429 377 5008 0.0752796 729148 chr6:70929843:->TCATCA COL9A1 NM_078485:c.1853-3059_1853-3058insTGATGA INTRON31 Benign rs147934773 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 6 1322 0.0045 47 1006 0.0467 14 694 0.0202 7 1008 0.0069 61 978 0.0624 135 5008 0.0269569 729149 chr6:70929843:TCA>- COL9A1 NM_078485:c.1853-3059_1853-3055delTGA INTRON31 Benign rs372560958 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 306 1322 0.2315 18 1006 0.0179 18 694 0.0259 14 1008 0.0139 10 978 0.0102 366 5008 0.0730831 729150 chr6:70929863:A>G COL9A1 NM_078485:c.1853-3079T>C INTRON31 Unknown significance rs771360944 This variant is a VUS because it does not have enough information. 729151 chr6:70929910:->G COL9A1 NM_078485:c.1853-3126_1853-3125insC INTRON31 Unknown significance rs398049030 This variant is a VUS because it does not have enough information. 729152 chr6:70929911:->T COL9A1 NM_078485:c.1853-3127_1853-3126insA INTRON31 Benign rs59262394 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 456 1322 0.3449 295 1006 0.2932 322 694 0.464 441 1008 0.4375 257 978 0.2628 1771 5008 0.353634 729153 chr6:70929911:G>T COL9A1 NM_078485:c.1853-3127C>A INTRON31 Unknown significance rs34892469 This variant is a VUS because it does not have enough information. 729154 chr6:70929911:GG>TGC COL9A1 Unknown significance rs386702484 This variant is a VUS because it does not have enough information. 729155 chr6:70929912:G>C COL9A1 NM_078485:c.1853-3128C>G INTRON31 Benign rs58885304 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 399 1322 0.3018 236 1006 0.2346 249 694 0.3588 333 1008 0.3304 216 978 0.2209 1433 5008 0.286142 729156 chr6:70929913:->C COL9A1 NM_078485:c.1853-3129_1853-3128insG INTRON31 Unknown significance rs200802448 This variant is a VUS because it does not have enough information. 729157 chr6:70929913:->TGC COL9A1 NM_078485:c.1853-3129_1853-3128insGCA INTRON31 Unknown significance rs398049030 This variant is a VUS because it does not have enough information. 729158 chr6:70929916:A>G COL9A1 NM_078485:c.1853-3132T>C INTRON31 Unknown significance rs534763131 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 729159 chr6:70929933:G>A COL9A1 NM_078485:c.1853-3149C>T INTRON31 Unknown significance rs139228201 This variant is a VUS because it does not have enough information. 5 1322 0.0038 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 6 5008 0.00119808 729160 chr6:70929946:T>G COL9A1 NM_078485:c.1853-3162A>C INTRON31 Unknown significance rs777118692 This variant is a VUS because it does not have enough information. 729161 chr6:70929949:T>C COL9A1 NM_078485:c.1853-3165A>G INTRON31 Unknown significance rs143255369 This variant is a VUS because it does not have enough information. 5 1322 0.0038 0 1006 0 0 694 0 0 1008 0 0 978 0 5 5008 0.000998403 729162 chr6:70930021:A>G COL9A1 NM_078485:c.1853-3237T>C INTRON31 Benign rs190549423 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 9 1322 0.0068 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 10 5008 0.00199681 729163 chr6:70930073:G>T COL9A1 NM_078485:c.1853-3289C>A INTRON31 Benign rs1200567 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 301 1322 0.2277 47 1006 0.0467 27 694 0.0389 6 1008 0.006 60 978 0.0613 441 5008 0.0880591 729164 chr6:70930077:->G COL9A1 NM_078485:c.1853-3293_1853-3292insC INTRON31 Benign rs150139945 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 294 1322 0.2224 0 1006 0 13 694 0.0187 0 1008 0 0 978 0 307 5008 0.0613019 729165 chr6:70930079:A>G COL9A1 NM_078485:c.1853-3295T>C INTRON31 Benign rs28694097 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 381 1322 0.2882 48 1006 0.0477 31 694 0.0447 6 1008 0.006 60 978 0.0613 526 5008 0.105032 729166 chr6:70930088:G>T COL9A1 NM_078485:c.1853-3304C>A INTRON31 Unknown significance rs539628320 This variant is a VUS because it does not have enough information. 5 1322 0.0038 0 1006 0 0 694 0 0 1008 0 0 978 0 5 5008 0.000998403 729167 chr6:70930093:->GTGT COL9A1 NM_078485:c.1853-3309_1853-3308insACAC INTRON31 Unknown significance rs58525634 This variant is a VUS because it does not have enough information. 729168 chr6:70930093:GT>- COL9A1 NM_078485:c.1853-3309_1853-3306delAC INTRON31 Unknown significance rs796970877 This variant is a VUS because it does not have enough information. 729169 chr6:70930093:GTGT>- COL9A1 NM_078485:c.1853-3309_1853-3304delACAC INTRON31 Unknown significance rs71749691 This variant is a VUS because it does not have enough information. 729170 chr6:70930093:GTGTGT>- COL9A1 NM_078485:c.1853-3309_1853-3302delACACAC INTRON31 Unknown significance rs72155096 This variant is a VUS because it does not have enough information. 729171 chr6:70930093:GTGTGTGT>- COL9A1 NM_078485:c.1853-3309_1853-3300delACACACAC INTRON31 Unknown significance rs796404376 This variant is a VUS because it does not have enough information. 729172 chr6:70930094:->GT COL9A1 NM_078485:c.1853-3310_1853-3309insAC INTRON31 Unknown significance rs71925903 This variant is a VUS because it does not have enough information. 729173 chr6:70930116:T>G COL9A1 NM_078485:c.1853-3332A>C INTRON31 Unknown significance rs372974173 This variant is a VUS because it does not have enough information. 729174 chr6:70930117:GTG>- COL9A1 NM_078485:c.1853-3333_1853-3329delCAC INTRON31 Unknown significance rs779178275 This variant is a VUS because it does not have enough information. 729175 chr6:70930117:GTGTGG>- COL9A1 NM_078485:c.1853-3333_1853-3326delCCACAC INTRON31 Unknown significance rs763362636 This variant is a VUS because it does not have enough information. 729176 chr6:70930167:C>G COL9A1 NM_078485:c.1853-3383G>C INTRON31 Benign rs539975140 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 0 1322 0 0 1006 0 0 694 0 0 1008 0 16 978 0.0164 16 5008 0.00319489 729177 chr6:70930233:T>C COL9A1 NM_078485:c.1853-3449A>G INTRON31 Unknown significance rs371642043 This variant is a VUS because it does not have enough information. 729178 chr6:70930242:G>A COL9A1 NM_078485:c.1853-3458C>T INTRON31 Unknown significance rs775544490 This variant is a VUS because it does not have enough information. 729179 chr6:70930257:AGAAATACCAG>- COL9A1 NM_078485:c.1853-3473_1853-3461delCTGGTATTTCT INTRON31 Unknown significance rs529376743 This variant is a VUS because it does not have enough information. 5 1322 0.0038 0 1006 0 0 694 0 0 1008 0 0 978 0 5 5008 0.000998403 729180 chr6:70930269:G>A COL9A1 NM_078485:c.1853-3485C>T INTRON31 Unknown significance rs74946925 This variant is a VUS because it does not have enough information. 729181 chr6:70930270:A>G COL9A1 NM_078485:c.1853-3486T>C INTRON31 Unknown significance rs190019541 This variant is a VUS because it does not have enough information. 0 1322 0 2 1006 0.002 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361 729182 chr6:70930288:C>G COL9A1 NM_078485:c.1853-3504G>C INTRON31 Unknown significance rs562990686 This variant is a VUS because it does not have enough information. 729183 chr6:70930288:C>T COL9A1 NM_078485:c.1853-3504G>A INTRON31 Unknown significance rs562990686 This variant is a VUS because it does not have enough information. 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 729184 chr6:70930289:AT>- COL9A1 NM_078485:c.1853-3505_1853-3502delAT INTRON31 Benign rs147184570 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 301 1322 0.2277 47 1006 0.0467 27 694 0.0389 7 1008 0.0069 61 978 0.0624 443 5008 0.0884585 729185 chr6:70930327:G>T COL9A1 NM_078485:c.1853-3543C>A INTRON31 Unknown significance rs561641003 This variant is a VUS because it does not have enough information. 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 729186 chr6:70930330:T>C COL9A1 NM_078485:c.1853-3546A>G INTRON31 Unknown significance rs575132672 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681 729187 chr6:70930407:A>C COL9A1 NM_078485:c.1853-3623T>G INTRON31 Unknown significance rs763228947 This variant is a VUS because it does not have enough information. 729188 chr6:70930421:C>T COL9A1 NM_078485:c.1853-3637G>A INTRON31 Benign rs16868775 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 80 1322 0.0605 252 1006 0.2505 293 694 0.4222 437 1008 0.4335 196 978 0.2004 1258 5008 0.251198 729189 chr6:70930429:C>T COL9A1 NM_078485:c.1853-3645G>A INTRON31 Benign rs369314981 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 0 1322 0 0 1006 0 0 694 0 0 1008 0 10 978 0.0102 10 5008 0.00199681 729190 chr6:70930541:C>T COL9A1 NM_078485:c.1853-3757G>A INTRON31 Unknown significance rs532692113 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 729191 chr6:70930595:T>G COL9A1 NM_078485:c.1853-3811A>C INTRON31 Unknown significance rs546106909 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361 729192 chr6:70930600:T>C COL9A1 NM_078485:c.1853-3816A>G INTRON31 Benign rs540654 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 302 1322 0.2284 48 1006 0.0477 27 694 0.0389 7 1008 0.0069 61 978 0.0624 445 5008 0.0888578 729193 chr6:70930641:A>G COL9A1 NM_078485:c.1853-3857T>C INTRON31 Unknown significance rs528670189 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681 729194 chr6:70930649:A>T COL9A1 NM_078485:c.1853-3865T>A INTRON31 Unknown significance rs546896150 This variant is a VUS because it does not have enough information. 729195 chr6:70930669:T>C COL9A1 NM_078485:c.1853-3885A>G INTRON31 Unknown significance rs181043242 This variant is a VUS because it does not have enough information. 1 1322 0.0008 1 1006 0.001 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361 729196 chr6:70930673:T>C COL9A1 NM_078485:c.1853-3889A>G INTRON31 Unknown significance rs568506077 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681 729197 chr6:70930697:ATTATGTA>- COL9A1 NM_078485:c.1853-3913_1853-3904delTACATAAT INTRON31 Unknown significance rs532657922 This variant is a VUS because it does not have enough information. 729198 chr6:70930720:C>T COL9A1 NM_078485:c.1853-3936G>A INTRON31 Unknown significance rs530924223 This variant is a VUS because it does not have enough information. 3 1322 0.0023 0 1006 0 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042 729199 chr6:70930761:C>T COL9A1 NM_078485:c.1853-3977G>A INTRON31 Unknown significance rs754695971 This variant is a VUS because it does not have enough information. 729200 chr6:70930801:->CA COL9A1 NM_078485:c.1853-4017_1853-4016insTG INTRON31 Unknown significance rs758619700 This variant is a VUS because it does not have enough information. 729201 chr6:70930801:G>- COL9A1 NM_078485:c.1853-4017delC INTRON31 Unknown significance rs766176027 This variant is a VUS because it does not have enough information. 729202 chr6:70930802:T>- COL9A1 NM_078485:c.1853-4018delA INTRON31 Benign rs58207213 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 310 1322 0.2345 52 1006 0.0517 33 694 0.0476 16 1008 0.0159 70 978 0.0716 481 5008 0.0960463 729203 chr6:70930811:T>A COL9A1 NM_078485:c.1853-4027A>T INTRON31 Benign rs185563256 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 11 1322 0.0083 20 1006 0.0199 6 694 0.0086 2 1008 0.002 2 978 0.002 41 5008 0.0081869 729204 chr6:70930888:G>A COL9A1 NM_078485:c.1853-4104C>T INTRON31 Unknown significance rs747818184 This variant is a VUS because it does not have enough information. 729205 chr6:70930892:G>A COL9A1 NM_078485:c.1853-4108C>T INTRON31 Benign rs9446211 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 79 1322 0.0598 1 1006 0.001 4 694 0.0058 0 1008 0 0 978 0 84 5008 0.0167732 729206 chr6:70930894:A>C COL9A1 NM_078485:c.1853-4110T>G INTRON31 Benign rs7739562 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 82 1322 0.062 253 1006 0.2515 292 694 0.4207 437 1008 0.4335 200 978 0.2045 1264 5008 0.252396 729207 chr6:70930897:A>T COL9A1 NM_078485:c.1853-4113T>A INTRON31 Unknown significance rs189582297 This variant is a VUS because it does not have enough information. 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681 729208 chr6:70930907:C>A COL9A1 NM_078485:c.1853-4123G>T INTRON31 Unknown significance rs569305235 This variant is a VUS because it does not have enough information. 729209 chr6:70930935:G>A COL9A1 NM_078485:c.1853-4151C>T INTRON31 Benign rs79979095 This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005. 98 1322 0.0741 0 1006 0 1 694 0.0014 0 1008 0 3 978 0.0031 102 5008 0.0203674 729210 chr6:70930995:G>C COL9A1 NM_078485:c.1853-4211C>G INTRON31 Unknown significance rs182150578 This variant is a VUS because it does not have enough information. 0<