688392
chr6:24172025:T>C
DCDC2
NM_016356:c.*2933A>G
THREE_PRIME_EXON
Unknown significance
rs369093030
This variant is a VUS because it does not have enough information.
688393
chr6:24172079:A>G
DCDC2
NM_016356:c.*2879T>C
THREE_PRIME_EXON
Unknown significance
rs191266340
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
688394
chr6:24172125:T>A
DCDC2
NM_016356:c.*2833A>T
THREE_PRIME_EXON
Unknown significance
rs528312638
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
688395
chr6:24172137:G>C
DCDC2
NM_016356:c.*2821C>G
THREE_PRIME_EXON
Unknown significance
rs551229958
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
688396
chr6:24172157:T>C
DCDC2
NM_016356:c.*2801A>G
THREE_PRIME_EXON
Unknown significance
rs765315104
This variant is a VUS because it does not have enough information.
688397
chr6:24172183:A>G
DCDC2
NM_016356:c.*2775T>C
THREE_PRIME_EXON
Unknown significance
rs571194141
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
688398
chr6:24172193:C>T
DCDC2
NM_016356:c.*2765G>A
THREE_PRIME_EXON
Unknown significance
rs181069294
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
688399
chr6:24172194:G>A
DCDC2
NM_016356:c.*2764C>T
THREE_PRIME_EXON
Unknown significance
rs370186102
This variant is a VUS because it does not have enough information.
688400
chr6:24172221:T>C
DCDC2
NM_016356:c.*2737A>G
THREE_PRIME_EXON
Unknown significance
rs758196218
This variant is a VUS because it does not have enough information.
688401
chr6:24172234:A>G
DCDC2
NM_016356:c.*2724T>C
THREE_PRIME_EXON
Benign
rs550559091
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
688402
chr6:24172241:G>A
DCDC2
NM_016356:c.*2717C>T
THREE_PRIME_EXON
Unknown significance
rs567659287
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
688403
chr6:24172244:T>C
DCDC2
NM_016356:c.*2714A>G
THREE_PRIME_EXON
Benign
rs142240923
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
27
1322
0.0204
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
28
5008
0.00559105
688404
chr6:24172245:G>C
DCDC2
NM_016356:c.*2713C>G
THREE_PRIME_EXON
Benign
rs114468662
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
33
1322
0.025
0
1006
0
2
694
0.0029
21
1008
0.0208
4
978
0.0041
60
5008
0.0119808
688405
chr6:24172312:C>T
DCDC2
NM_016356:c.*2646G>A
THREE_PRIME_EXON
Unknown significance
rs566917433
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
688406
chr6:24172313:G>A
DCDC2
NM_016356:c.*2645C>T
THREE_PRIME_EXON
Unknown significance
rs777612229
This variant is a VUS because it does not have enough information.
688407
chr6:24172322:C>T
DCDC2
NM_016356:c.*2636G>A
THREE_PRIME_EXON
Unknown significance
rs539204731
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
688408
chr6:24172331:C>G
DCDC2
NM_016356:c.*2627G>C
THREE_PRIME_EXON
Benign
rs185396049
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
2
694
0.0029
0
1008
0
0
978
0
7
5008
0.00139776
688409
chr6:24172340:->AAC
DCDC2
NM_016356:c.*2618_*2619insGTT
THREE_PRIME_EXON
Unknown significance
rs138619994
This variant is a VUS because it does not have enough information.
688410
chr6:24172347:A>T
DCDC2
NM_016356:c.*2611T>A
THREE_PRIME_EXON
Unknown significance
rs576003796
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
688411
chr6:24172348:T>G
DCDC2
NM_016356:c.*2610A>C
THREE_PRIME_EXON
Unknown significance
rs544959947
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
688412
chr6:24172366:T>C
DCDC2
NM_016356:c.*2592A>G
THREE_PRIME_EXON
Unknown significance
rs190602092
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
688413
chr6:24172374:T>A
DCDC2
NM_016356:c.*2584A>T
THREE_PRIME_EXON
Benign
rs41304906
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
1
1322
0.0008
20
1006
0.0199
9
694
0.013
2
1008
0.002
48
978
0.0491
80
5008
0.0159744
688414
chr6:24172378:T>C
DCDC2
NM_016356:c.*2580A>G
THREE_PRIME_EXON
Unknown significance
rs542333299
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
688415
chr6:24172392:C>G
DCDC2
NM_016356:c.*2566G>C
THREE_PRIME_EXON
Unknown significance
rs543303607
This variant is a VUS because it does not have enough information.
688416
chr6:24172397:G>C
DCDC2
NM_016356:c.*2561C>G
THREE_PRIME_EXON
Unknown significance
rs774062828
This variant is a VUS because it does not have enough information.
688417
chr6:24172424:G>C
DCDC2
NM_016356:c.*2534C>G
THREE_PRIME_EXON
Unknown significance
rs761651635
This variant is a VUS because it does not have enough information.
688418
chr6:24172451:->T
DCDC2
NM_016356:c.*2507_*2508insA
THREE_PRIME_EXON
Unknown significance
rs561595835
This variant is a VUS because it does not have enough information.
688419
chr6:24172455:T>C
DCDC2
NM_016356:c.*2503A>G
THREE_PRIME_EXON
Unknown significance
rs559417992
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
688420
chr6:24172488:A>G
DCDC2
NM_016356:c.*2470T>C
THREE_PRIME_EXON
Benign
rs78473954
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
9
1008
0.0089
0
978
0
9
5008
0.00179712
688421
chr6:24172526:G>A
DCDC2
NM_016356:c.*2432C>T
THREE_PRIME_EXON
Benign
rs41304913
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
1
1322
0.0008
18
1006
0.0179
1
694
0.0014
0
1008
0
0
978
0
20
5008
0.00399361
688422
chr6:24172553:G>A
DCDC2
NM_016356:c.*2405C>T
THREE_PRIME_EXON
Unknown significance
rs749320457
This variant is a VUS because it does not have enough information.
688423
chr6:24172577:C>T
DCDC2
NM_016356:c.*2381G>A
THREE_PRIME_EXON
Unknown significance
rs760469207
This variant is a VUS because it does not have enough information.
688424
chr6:24172589:T>-
DCDC2
NM_016356:c.*2369delA
THREE_PRIME_EXON
Unknown significance
rs562721341
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
1
978
0.001
4
5008
0.000798722
688425
chr6:24172620:C>T
DCDC2
NM_016356:c.*2338G>A
THREE_PRIME_EXON
Benign
rs60947379
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
64
1322
0.0484
2
1006
0.002
2
694
0.0029
0
1008
0
0
978
0
68
5008
0.0135783
688426
chr6:24172667:T>C
DCDC2
NM_016356:c.*2291A>G
THREE_PRIME_EXON
Benign
rs61431152
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
62
1322
0.0469
2
1006
0.002
2
694
0.0029
0
1008
0
0
978
0
66
5008
0.0131789
688427
chr6:24172694:C>T
DCDC2
NM_016356:c.*2264G>A
THREE_PRIME_EXON
Unknown significance
rs150770243
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
688428
chr6:24172734:T>C
DCDC2
NM_016356:c.*2224A>G
THREE_PRIME_EXON
Unknown significance
rs561096095
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
688429
chr6:24172735:G>A
DCDC2
NM_016356:c.*2223C>T
THREE_PRIME_EXON
Benign
rs139147469
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
0
694
0
4
1008
0.004
51
978
0.0521
64
5008
0.0127796
688430
chr6:24172746:C>T
DCDC2
NM_016356:c.*2212G>A
THREE_PRIME_EXON
Benign
rs12333271
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
654
1322
0.4947
25
1006
0.0249
38
694
0.0548
0
1008
0
0
978
0
717
5008
0.143171
688431
chr6:24172748:G>T
DCDC2
NM_016356:c.*2210C>A
THREE_PRIME_EXON
Unknown significance
rs566932974
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
688432
chr6:24172780:AAAGAG>-
DCDC2
NM_016356:c.*2178_*2185delCTCTTT
THREE_PRIME_EXON
Unknown significance
rs796955072
This variant is a VUS because it does not have enough information.
688433
chr6:24172802:T>C
DCDC2
NM_016356:c.*2156A>G
THREE_PRIME_EXON
Unknown significance
rs539180371
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
688434
chr6:24172804:G>A
DCDC2
NM_016356:c.*2154C>T
THREE_PRIME_EXON
Unknown significance
rs565352952
This variant is a VUS because it does not have enough information.
688435
chr6:24172811:C>G
DCDC2
NM_016356:c.*2147G>C
THREE_PRIME_EXON
Benign
rs12333304
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
322
1322
0.2436
4
1006
0.004
13
694
0.0187
0
1008
0
0
978
0
339
5008
0.0676917
688436
chr6:24172823:A>G
DCDC2
NM_016356:c.*2135T>C
THREE_PRIME_EXON
Unknown significance
rs368586909
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
688437
chr6:24172834:T>C
DCDC2
NM_016356:c.*2124A>G
THREE_PRIME_EXON
Unknown significance
rs751927251
This variant is a VUS because it does not have enough information.
688438
chr6:24172836:G>C
DCDC2
NM_016356:c.*2122C>G
THREE_PRIME_EXON
Unknown significance
rs532646434
This variant is a VUS because it does not have enough information.
688439
chr6:24172846:C>T
DCDC2
NM_016356:c.*2112G>A
THREE_PRIME_EXON
Unknown significance
rs538495462
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
688440
chr6:24172850:C>T
DCDC2
NM_016356:c.*2108G>A
THREE_PRIME_EXON
Unknown significance
rs781345816
This variant is a VUS because it does not have enough information.
688441
chr6:24172869:A>-
DCDC2
NM_016356:c.*2089delT
THREE_PRIME_EXON
Benign
rs149156540
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
321
1322
0.2428
4
1006
0.004
13
694
0.0187
0
1008
0
0
978
0
338
5008
0.067492
688442
chr6:24172926:A>G
DCDC2
NM_016356:c.*2032T>C
THREE_PRIME_EXON
Benign
rs6937665
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
91
1322
0.0688
162
1006
0.161
167
694
0.2406
574
1008
0.5694
260
978
0.2658
1254
5008
0.250399
688443
chr6:24172948:G>A
DCDC2
NM_016356:c.*2010C>T
THREE_PRIME_EXON
Unknown significance
rs182866125
This variant is a VUS because it does not have enough information.
688444
chr6:24172962:C>A
DCDC2
NM_016356:c.*1996G>T
THREE_PRIME_EXON
Benign
rs1832709
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
11
1322
0.0083
110
1006
0.1093
86
694
0.1239
195
1008
0.1935
151
978
0.1544
553
5008
0.110423
688445
chr6:24172993:G>A
DCDC2
NM_016356:c.*1965C>T
THREE_PRIME_EXON
Unknown significance
rs780146737
This variant is a VUS because it does not have enough information.
688446
chr6:24172996:C>T
DCDC2
NM_016356:c.*1962G>A
THREE_PRIME_EXON
Unknown significance
rs188928127
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
688447
chr6:24173038:A>G
DCDC2
NM_016356:c.*1920T>C
THREE_PRIME_EXON
Unknown significance
rs192133478
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
688448
chr6:24173039:T>G
DCDC2
NM_016356:c.*1919A>C
THREE_PRIME_EXON
Unknown significance
rs572892371
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
688449
chr6:24173090:G>T
DCDC2
NM_016356:c.*1868C>A
THREE_PRIME_EXON
Unknown significance
rs770665971
This variant is a VUS because it does not have enough information.
688450
chr6:24173091:C>G
DCDC2
NM_016356:c.*1867G>C
THREE_PRIME_EXON
Benign
rs149893351
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
64
1322
0.0484
2
1006
0.002
2
694
0.0029
0
1008
0
0
978
0
68
5008
0.0135783
688451
chr6:24173137:C>T
DCDC2
NM_016356:c.*1821G>A
THREE_PRIME_EXON
Unknown significance
rs564690715
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
688452
chr6:24173189:G>A
DCDC2
NM_016356:c.*1769C>T
THREE_PRIME_EXON
Unknown significance
rs536276033
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
688453
chr6:24173192:G>A
DCDC2
NM_016356:c.*1766C>T
THREE_PRIME_EXON
Benign
rs1832708
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
287
1322
0.2171
522
1006
0.5189
297
694
0.428
210
1008
0.2083
371
978
0.3793
1687
5008
0.336861
688454
chr6:24173199:G>A
DCDC2
NM_016356:c.*1759C>T
THREE_PRIME_EXON
Unknown significance
rs561219227
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
688455
chr6:24173218:->AAT
DCDC2
NM_016356:c.*1740_*1741insATT
THREE_PRIME_EXON
Unknown significance
rs751566899
This variant is a VUS because it does not have enough information.
688456
chr6:24173218:->AATAATAATAAT
DCDC2
NM_016356:c.*1740_*1741insATTATTATTATT
THREE_PRIME_EXON
Unknown significance
rs10529373
This variant is a VUS because it does not have enough information.
688457
chr6:24173218:->AATAATAATAATAAT
DCDC2
NM_016356:c.*1740_*1741insATTATTATTATTATT
THREE_PRIME_EXON
Unknown significance
rs10529373
This variant is a VUS because it does not have enough information.
688458
chr6:24173218:->AATAATAATAATAATAAT
DCDC2
NM_016356:c.*1740_*1741insATTATTATTATTATTATT
THREE_PRIME_EXON
Unknown significance
rs59837095
This variant is a VUS because it does not have enough information.
688459
chr6:24173218:->TAATAATAAT
DCDC2
NM_016356:c.*1740_*1741insATTATTATTA
THREE_PRIME_EXON
Unknown significance
rs10529373
This variant is a VUS because it does not have enough information.
688460
chr6:24173218:AATAAT>-
DCDC2
NM_016356:c.*1740_*1747delATTATT
THREE_PRIME_EXON
Unknown significance
rs151242509
This variant is a VUS because it does not have enough information.
688461
chr6:24173220:T>A
DCDC2
NM_016356:c.*1738A>T
THREE_PRIME_EXON
Benign
rs41271771
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
46
1322
0.0348
34
1006
0.0338
10
694
0.0144
3
1008
0.003
43
978
0.044
136
5008
0.0271565
688462
chr6:24173223:T>A
DCDC2
NM_016356:c.*1735A>T
THREE_PRIME_EXON
Benign
rs546967099
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
154
1322
0.1165
14
1006
0.0139
11
694
0.0159
1
1008
0.001
28
978
0.0286
208
5008
0.0415335
688463
chr6:24173247:->TAG
DCDC2
NM_016356:c.*1711_*1712insCTA
THREE_PRIME_EXON
Unknown significance
rs560469021
This variant is a VUS because it does not have enough information.
688464
chr6:24173250:A>T
DCDC2
NM_016356:c.*1708T>A
THREE_PRIME_EXON
Unknown significance
rs560323772
This variant is a VUS because it does not have enough information.
0
1322
0
1
1006
0.001
3
694
0.0043
1
1008
0.001
0
978
0
5
5008
0.000998403
688465
chr6:24173269:C>T
DCDC2
NM_016356:c.*1689G>A
THREE_PRIME_EXON
Benign
rs6938529
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
91
1322
0.0688
163
1006
0.162
167
694
0.2406
572
1008
0.5675
258
978
0.2638
1251
5008
0.2498
688466
chr6:24173273:C>G
DCDC2
NM_016356:c.*1685G>C
THREE_PRIME_EXON
Benign
rs4236030
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
1321
1322
0.9992
1006
1006
1
694
694
1
1008
1008
1
978
978
1
5007
5008
0.9998
688467
chr6:24173325:A>-
DCDC2
NM_016356:c.*1633delT
THREE_PRIME_EXON
Unknown significance
rs35130856
This variant is a VUS because it does not have enough information.
688468
chr6:24173326:A>C
DCDC2
NM_016356:c.*1632T>G
THREE_PRIME_EXON
Unknown significance
rs555942419
This variant is a VUS because it does not have enough information.
688469
chr6:24173334:C>T
DCDC2
NM_016356:c.*1624G>A
THREE_PRIME_EXON
Benign
rs9467061
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
314
1322
0.2375
4
1006
0.004
13
694
0.0187
0
1008
0
0
978
0
331
5008
0.0660942
688470
chr6:24173362:A>G
DCDC2
NM_016356:c.*1596T>C
THREE_PRIME_EXON
Unknown significance
rs540295233
This variant is a VUS because it does not have enough information.
688471
chr6:24173382:T>C
DCDC2
NM_016356:c.*1576A>G
THREE_PRIME_EXON
Benign
rs9467062
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
655
1322
0.4955
25
1006
0.0249
38
694
0.0548
0
1008
0
0
978
0
718
5008
0.143371
688472
chr6:24173410:A>G
DCDC2
NM_016356:c.*1548T>C
THREE_PRIME_EXON
Unknown significance
rs776334137
This variant is a VUS because it does not have enough information.
688473
chr6:24173415:C>T
DCDC2
NM_016356:c.*1543G>A
THREE_PRIME_EXON
Unknown significance
rs560309108
This variant is a VUS because it does not have enough information.
688474
chr6:24173469:T>C
DCDC2
NM_016356:c.*1489A>G
THREE_PRIME_EXON
Benign
rs369117102
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
6
1008
0.006
1
978
0.001
7
5008
0.00139776
688475
chr6:24173511:T>C
DCDC2
NM_016356:c.*1447A>G
THREE_PRIME_EXON
Unknown significance
rs568716262
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
688476
chr6:24173524:G>C
DCDC2
NM_016356:c.*1434C>G
THREE_PRIME_EXON
Unknown significance
rs762894208
This variant is a VUS because it does not have enough information.
688477
chr6:24173561:T>C
DCDC2
NM_016356:c.*1397A>G
THREE_PRIME_EXON
Unknown significance
rs759108050
This variant is a VUS because it does not have enough information.
688478
chr6:24173582:G>A
DCDC2
NM_016356:c.*1376C>T
THREE_PRIME_EXON
Unknown significance
rs765049489
This variant is a VUS because it does not have enough information.
688479
chr6:24173585:A>G
DCDC2
NM_016356:c.*1373T>C
THREE_PRIME_EXON
Benign
rs7773379
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
654
1322
0.4947
25
1006
0.0249
38
694
0.0548
0
1008
0
0
978
0
717
5008
0.143171
688480
chr6:24173669:A>C
DCDC2
NM_016356:c.*1289T>G
THREE_PRIME_EXON
Unknown significance
rs552926330
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
688481
chr6:24173690:T>C
DCDC2
NM_016356:c.*1268A>G
THREE_PRIME_EXON
Unknown significance
rs757932461
This variant is a VUS because it does not have enough information.
688482
chr6:24173715:C>A
DCDC2
NM_016356:c.*1243G>T
THREE_PRIME_EXON
Benign
rs146459247
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
35
1322
0.0265
2
1006
0.002
2
694
0.0029
0
1008
0
0
978
0
39
5008
0.00778754
688483
chr6:24173730:C>A
DCDC2
NM_016356:c.*1228G>T
THREE_PRIME_EXON
Unknown significance
rs371980326
This variant is a VUS because it does not have enough information.
688484
chr6:24173741:C>T
DCDC2
NM_016356:c.*1217G>A
THREE_PRIME_EXON
Benign
rs7773748
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
654
1322
0.4947
25
1006
0.0249
38
694
0.0548
1
1008
0.001
1
978
0.001
719
5008
0.14357
688485
chr6:24173742:G>A
DCDC2
NM_016356:c.*1216C>T
THREE_PRIME_EXON
Unknown significance
rs561913362
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
688486
chr6:24173795:C>T
DCDC2
NM_016356:c.*1163G>A
THREE_PRIME_EXON
Unknown significance
rs529308252
This variant is a VUS because it does not have enough information.
688487
chr6:24173852:ATA>-
DCDC2
NM_016356:c.*1106_*1110delTAT
THREE_PRIME_EXON
Unknown significance
rs532519482
This variant is a VUS because it does not have enough information.
688488
chr6:24173914:T>G
DCDC2
NM_016356:c.*1044A>C
THREE_PRIME_EXON
Unknown significance
rs756662573
This variant is a VUS because it does not have enough information.
688489
chr6:24173935:C>T
DCDC2
NM_016356:c.*1023G>A
THREE_PRIME_EXON
Unknown significance
rs780525776
This variant is a VUS because it does not have enough information.
688490
chr6:24173961:T>C
DCDC2
NM_016356:c.*997A>G
THREE_PRIME_EXON
Unknown significance
rs571986675
This variant is a VUS because it does not have enough information.
688491
chr6:24174051:T>C
DCDC2
NM_016356:c.*907A>G
THREE_PRIME_EXON
Unknown significance
rs575029853
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
688492
chr6:24174073:TT>-
DCDC2
NM_016356:c.*885_*888delAA
THREE_PRIME_EXON
Unknown significance
rs779406738
This variant is a VUS because it does not have enough information.
688493
chr6:24174103:A>T
DCDC2
NM_016356:c.*855T>A
THREE_PRIME_EXON
Unknown significance
rs542294755
This variant is a VUS because it does not have enough information.
688494
chr6:24174107:T>A
DCDC2
NM_016356:c.*851A>T
THREE_PRIME_EXON
Benign
rs187768588
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
10
1322
0.0076
1
1006
0.001
0
694
0
0
1008
0
0
978
0
11
5008
0.00219649
688495
chr6:24174158:G>C
DCDC2
NM_016356:c.*800C>G
THREE_PRIME_EXON
Unknown significance
rs749432221
This variant is a VUS because it does not have enough information.
688496
chr6:24174186:G>A
DCDC2
NM_016356:c.*772C>T
THREE_PRIME_EXON
Benign
rs6901696
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
654
1322
0.4947
25
1006
0.0249
38
694
0.0548
0
1008
0
0
978
0
717
5008
0.143171
688497
chr6:24174189:C>T
DCDC2
NM_016356:c.*769G>A
THREE_PRIME_EXON
Unknown significance
rs574663923
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
688498
chr6:24174205:G>A
DCDC2
NM_016356:c.*753C>T
THREE_PRIME_EXON
Unknown significance
rs778798127
This variant is a VUS because it does not have enough information.
688499
chr6:24174219:G>A
DCDC2
NM_016356:c.*739C>T
THREE_PRIME_EXON
Unknown significance
rs760344796
This variant is a VUS because it does not have enough information.
688500
chr6:24174229:C>T
DCDC2
NM_016356:c.*729G>A
THREE_PRIME_EXON
Unknown significance
rs540163820
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
688501
chr6:24174231:T>A
DCDC2
NM_016356:c.*727A>T
THREE_PRIME_EXON
Benign
rs74607513
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
64
1322
0.0484
2
1006
0.002
2
694
0.0029
0
1008
0
0
978
0
68
5008
0.0135783
688502
chr6:24174245:T>C
DCDC2
NM_016356:c.*713A>G
THREE_PRIME_EXON
Unknown significance
rs772146703
This variant is a VUS because it does not have enough information.
688503
chr6:24174257:C>T
DCDC2
NM_016356:c.*701G>A
THREE_PRIME_EXON
Unknown significance
rs532574512
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
688504
chr6:24174284:C>T
DCDC2
NM_016356:c.*674G>A
THREE_PRIME_EXON
Benign
rs191842890
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
688505
chr6:24174285:G>A
DCDC2
NM_016356:c.*673C>T
THREE_PRIME_EXON
Benign
rs139799255
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
4
1008
0.004
51
978
0.0521
65
5008
0.0129792
688506
chr6:24174288:A>T
DCDC2
NM_016356:c.*670T>A
THREE_PRIME_EXON
Unknown significance
rs543989408
This variant is a VUS because it does not have enough information.
688507
chr6:24174299:A>G
DCDC2
NM_016356:c.*659T>C
THREE_PRIME_EXON
Unknown significance
rs773100378
This variant is a VUS because it does not have enough information.
688508
chr6:24174312:T>G
DCDC2
NM_016356:c.*646A>C
THREE_PRIME_EXON
Unknown significance
rs112295656
This variant is a VUS because it does not have enough information.
688509
chr6:24174329:C>G
DCDC2
NM_016356:c.*629G>C
THREE_PRIME_EXON
Benign
rs6456593
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
851
1322
0.6437
190
1006
0.1889
209
694
0.3012
588
1008
0.5833
263
978
0.2689
2101
5008
0.419529
688510
chr6:24174333:A>G
DCDC2
NM_016356:c.*625T>C
THREE_PRIME_EXON
Benign
rs6456594
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
851
1322
0.6437
190
1006
0.1889
209
694
0.3012
589
1008
0.5843
263
978
0.2689
2102
5008
0.419728
688511
chr6:24174349:C>T
DCDC2
NM_016356:c.*609G>A
THREE_PRIME_EXON
Unknown significance
rs776709051
This variant is a VUS because it does not have enough information.
688512
chr6:24174355:CT>-
DCDC2
NM_016356:c.*603_*606delAG
THREE_PRIME_EXON
Unknown significance
rs754024432
This variant is a VUS because it does not have enough information.
688513
chr6:24174377:A>C
DCDC2
NM_016356:c.*581T>G
THREE_PRIME_EXON
Benign
rs184297302
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
33
1322
0.025
0
1006
0
2
694
0.0029
0
1008
0
0
978
0
35
5008
0.00698882
688514
chr6:24174388:C>T
DCDC2
NM_016356:c.*570G>A
THREE_PRIME_EXON
Unknown significance
rs527947156
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
688515
chr6:24174389:G>A
DCDC2
NM_016356:c.*569C>T
THREE_PRIME_EXON
Benign
rs6456595
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
654
1322
0.4947
25
1006
0.0249
38
694
0.0548
0
1008
0
0
978
0
717
5008
0.143171
688516
chr6:24174389:GC>AA
DCDC2
Unknown significance
rs386698068
This variant is a VUS because it does not have enough information.
688517
chr6:24174390:C>A
DCDC2
NM_016356:c.*568G>T
THREE_PRIME_EXON
Benign
rs6456596
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
654
1322
0.4947
25
1006
0.0249
38
694
0.0548
0
1008
0
0
978
0
717
5008
0.143171
688518
chr6:24174404:T>C
DCDC2
NM_016356:c.*554A>G
THREE_PRIME_EXON
Unknown significance
rs530070009
This variant is a VUS because it does not have enough information.
688519
chr6:24174440:A>G
DCDC2
NM_016356:c.*518T>C
THREE_PRIME_EXON
Unknown significance
rs538232426
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
688520
chr6:24174447:G>T
DCDC2
NM_016356:c.*511C>A
THREE_PRIME_EXON
Unknown significance
rs774816129
This variant is a VUS because it does not have enough information.
688521
chr6:24174448:C>T
DCDC2
NM_016356:c.*510G>A
THREE_PRIME_EXON
Unknown significance
rs558158411
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
688522
chr6:24174487:T>A
DCDC2
NM_016356:c.*471A>T
THREE_PRIME_EXON
Unknown significance
rs762703982
This variant is a VUS because it does not have enough information.
688523
chr6:24174499:G>A
DCDC2
NM_016356:c.*459C>T
THREE_PRIME_EXON
Unknown significance
rs187084904
This variant is a VUS because it does not have enough information.
688524
chr6:24174507:G>A
DCDC2
NM_016356:c.*451C>T
THREE_PRIME_EXON
Unknown significance
rs546897493
This variant is a VUS because it does not have enough information.
688525
chr6:24174541:C>T
DCDC2
NM_016356:c.*417G>A
THREE_PRIME_EXON
Unknown significance
rs548198878
This variant is a VUS because it does not have enough information.
688526
chr6:24174591:C>T
DCDC2
NM_016356:c.*367G>A
THREE_PRIME_EXON
Unknown significance
rs112757771
This variant is a VUS because it does not have enough information.
688527
chr6:24174613:T>A
DCDC2
NM_016356:c.*345A>T
THREE_PRIME_EXON
Unknown significance
rs192341566
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
688528
chr6:24174648:G>A
DCDC2
NM_016356:c.*310C>T
THREE_PRIME_EXON
Unknown significance
rs537581124
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
0
1008
0
4
978
0.0041
4
5008
0.000798722
688529
chr6:24174666:T>C
DCDC2
NM_016356:c.*292A>G
THREE_PRIME_EXON
Unknown significance
rs554707580
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
688530
chr6:24174674:A>G
DCDC2
NM_016356:c.*284T>C
THREE_PRIME_EXON
Benign
rs16888768
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
47
1322
0.0356
8
1006
0.008
6
694
0.0086
0
1008
0
0
978
0
61
5008
0.0121805
688531
chr6:24174680:->TACAAA
DCDC2
NM_016356:c.*278_*279insTTTGTA
THREE_PRIME_EXON
Benign
rs10636186
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
850
1322
0.643
186
1006
0.1849
208
694
0.2997
582
1008
0.5774
263
978
0.2689
2089
5008
0.417133
688532
chr6:24174681:->TACAAA
DCDC2
NM_016356:c.*277_*278insTTTGTA
THREE_PRIME_EXON
Unknown significance
rs34175698
This variant is a VUS because it does not have enough information.
688533
chr6:24174685:G>A
DCDC2
NM_016356:c.*273C>T
THREE_PRIME_EXON
Unknown significance
rs201809976
This variant is a VUS because it does not have enough information.
688534
chr6:24174688:G>T
DCDC2
NM_016356:c.*270C>A
THREE_PRIME_EXON
Unknown significance
rs540494095
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
688535
chr6:24174733:TATTTC>-
DCDC2
NM_016356:c.*225_*232delGAAATA
THREE_PRIME_EXON
Unknown significance
rs781039306
This variant is a VUS because it does not have enough information.
688536
chr6:24174759:T>G
DCDC2
NM_016356:c.*199A>C
THREE_PRIME_EXON
Unknown significance
rs554125844
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
688537
chr6:24174760:G>T
DCDC2
NM_016356:c.*198C>A
THREE_PRIME_EXON
Unknown significance
rs577247114
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
688538
chr6:24174803:A>C
DCDC2
NM_016356:c.*155T>G
THREE_PRIME_EXON
Benign
rs7744665
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
654
1322
0.4947
25
1006
0.0249
38
694
0.0548
0
1008
0
0
978
0
717
5008
0.143171
688539
chr6:24174834:T>A
DCDC2
NM_016356:c.*124A>T
THREE_PRIME_EXON
Benign
rs7764902
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
654
1322
0.4947
25
1006
0.0249
38
694
0.0548
0
1008
0
0
978
0
717
5008
0.143171
688540
chr6:24174840:G>A
DCDC2
NM_016356:c.*118C>T
THREE_PRIME_EXON
Unknown significance
rs538484732
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
688541
chr6:24174850:T>A
DCDC2
NM_016356:c.*108A>T
THREE_PRIME_EXON
Unknown significance
rs3747780
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
4
1008
0.004
0
978
0
4
5008
0.000798722
688542
chr6:24174852:C>T
DCDC2
NM_016356:c.*106G>A
THREE_PRIME_EXON
Unknown significance
rs185251729
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
688543
chr6:24174886:A>G
DCDC2
NM_016356:c.*72T>C
THREE_PRIME_EXON
Unknown significance
rs371713513
This variant is a VUS because it does not have enough information.
688544
chr6:24174902:A>G
DCDC2
NM_016356:c.*56T>C
THREE_PRIME_EXON
Unknown significance
rs527895036
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
688545
chr6:24174909:T>C
DCDC2
NM_016356:c.*49A>G
THREE_PRIME_EXON
Unknown significance
rs367609076
This variant is a VUS because it does not have enough information.
0
8600
0
4
4404
0.000908265
4
13004
0.000307598
10
10374
0.000963948
0
11496
0
0
8428
0
0
6598
0
0
66152
0
0
904
0
0
16266
0
10
120218
8.31822e-05
688546
chr6:24174912:C>A
DCDC2
NM_016356:c.*46G>T
THREE_PRIME_EXON
Unknown significance
rs752077093
This variant is a VUS because it does not have enough information.
0
10374
0
0
11498
0
1
8428
0.000118652
0
6598
0
1
66174
1.51117e-05
0
904
0
0
16248
0
2
120224
1.66356e-05
688547
chr6:24174924:C>T
DCDC2
NM_016356:c.*34G>A
THREE_PRIME_EXON
Unknown significance
rs11557307
This variant is a VUS because it does not have enough information.
688548
chr6:24174928:C>T
DCDC2
NM_016356:c.*30G>A
THREE_PRIME_EXON
Unknown significance
rs755647628
This variant is a VUS because it does not have enough information.
3
10382
0.000288962
1
11516
8.68357e-05
0
8490
0
0
6606
0
0
66342
0
0
904
0
0
16338
0
4
120578
3.31735e-05
688549
chr6:24174929:G>A
DCDC2
NM_016356:c.*29C>T
THREE_PRIME_EXON
Unknown significance
rs765897825
This variant is a VUS because it does not have enough information.
0
10388
0
0
11530
0
1
8502
0.000117619
0
6610
0
1
66396
1.50611e-05
0
906
0
0
16366
0
2
120698
1.65703e-05
688550
chr6:24174932:C>A
DCDC2
NM_016356:c.*26G>T
THREE_PRIME_EXON
Unknown significance
rs755428064
This variant is a VUS because it does not have enough information.
688551
chr6:24174935:T>C
DCDC2
NM_016356:c.*23A>G
THREE_PRIME_EXON
Unknown significance
rs532161746
This variant is a VUS because it does not have enough information.
688552
chr6:24174937:T>A
DCDC2
NM_016356:c.*21A>T
THREE_PRIME_EXON
Unknown significance
rs753227406
This variant is a VUS because it does not have enough information.
0
10398
0
1
11540
8.66551e-05
0
8566
0
0
6612
0
0
66530
0
0
906
0
0
16438
0
1
120990
8.26515e-06
688553
chr6:24174937:T>C
DCDC2
NM_016356:c.*21A>G
THREE_PRIME_EXON
Unknown significance
rs753227406
This variant is a VUS because it does not have enough information.
0
10398
0
0
11540
0
1
8566
0.000116741
0
6612
0
0
66530
0
0
906
0
0
16438
0
1
120990
8.26515e-06
688555
chr6:24174939:C>T
DCDC2
NM_016356:c.*19G>A
THREE_PRIME_EXON
Unknown significance
rs548002913
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
0
10398
0
0
11536
0
0
8580
0
0
6610
0
0
66538
0
0
904
0
5
16434
0.000304247
5
121000
4.13223e-05
688554
chr6:24174939:CT>-
DCDC2
NM_016356:c.*19_*22delAG
THREE_PRIME_EXON
Unknown significance
rs747311373
This variant is a VUS because it does not have enough information.
688556
chr6:24174944:T>C
DCDC2
NM_016356:c.*14A>G
THREE_PRIME_EXON
Unknown significance
rs747975346
This variant is a VUS because it does not have enough information.
0
10402
0
0
11560
0
0
8604
0
0
6612
0
1
66596
1.50159e-05
0
906
0
0
16456
0
1
121136
8.25518e-06
688557
chr6:24174946:T>C
DCDC2
NM_016356:c.*12A>G
THREE_PRIME_EXON
Unknown significance
rs758240952
This variant is a VUS because it does not have enough information.
0
10402
0
3
11562
0.000259471
0
8614
0
0
6612
0
0
66598
0
0
906
0
0
16476
0
3
121170
2.47586e-05
688558
chr6:24174947:T>C
DCDC2
NM_016356:c.*11A>G
THREE_PRIME_EXON
Unknown significance
rs777894957
This variant is a VUS because it does not have enough information.
0
10402
0
0
11562
0
0
8610
0
0
6612
0
1
66592
1.50168e-05
0
906
0
0
16468
0
1
121152
8.25409e-06
688559
chr6:24174955:G>C
DCDC2
NM_016356:c.*3C>G
THREE_PRIME_EXON
Benign
rs9358755
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
7023
8600
0.816628
2119
4406
0.480935
9142
13006
0.702906
531
1322
0.4017
814
1006
0.8091
566
694
0.8156
980
1008
0.9722
865
978
0.8845
3756
5008
0.75
4828
10404
0.464052
10090
11576
0.871631
8417
8652
0.972839
6191
6614
0.936045
54725
66720
0.820219
756
908
0.832599
14592
16508
0.883935
99599
121382
0.820542
688560
chr6:24174966:C>T
DCDC2
NM_016356:p.Val475Met
NM_016356:c.1423G>A
EXON10
Unknown significance
rs145154884
This variant is a VUS because it does not have enough information.
0.065
N
0.004;0.003
D
0.943;1.0
P;D
0.101557
N
0.640425
N;N
3.86
C
3
8600
0.000348837
12
4406
0.00272356
15
13006
0.00115331
3
1322
0.0023
1
1006
0.001
0
694
0
0
1008
0
1
978
0.001
5
5008
0.000998403
22
10404
0.00211457
4
11578
0.000345483
0
8650
0
0
6614
0
9
66720
0.000134892
0
908
0
1
16502
6.05987e-05
36
121376
0.000296599
688561
chr6:24174967:G>A
DCDC2
NM_016356:p.Ala474Ala
NM_016356:c.1422C>T
EXON10
Unknown significance
rs146868469
This variant is a VUS because it does not have enough information.
1
8600
0.000116279
1
4406
0.000226963
2
13006
0.000153775
2
10404
0.000192234
0
11576
0
0
8652
0
0
6614
0
4
66720
5.9952e-05
0
908
0
0
16506
0
6
121380
4.94315e-05
688562
chr6:24174984:T>G
DCDC2
NM_016356:p.Asn469His
NM_016356:c.1405A>C
EXON10
Likely benign
rs140626877
Pathogenicity is based on prediction data only. 2 out of 6 predictions were pathogenic.
-0.222
N
0.063;0.034
T;D
0.001;0.013
B
0.295089
N
0.999936
N;N
3.28
C
1
8600
0.000116279
0
4406
0
1
13006
7.68876e-05
688563
chr6:24174993:T>C
DCDC2
NM_016356:p.Asn466Asp
NM_016356:c.1396A>G
EXON10
Likely benign
rs745898766
Pathogenicity is based on prediction data only. 1 out of 6 predictions were pathogenic.
0.114
N
0.113;0.065
T
0.001;0.082
B
0.191656
N
1
N;N
1.73
C
0
10404
0
0
11578
0
0
8654
0
0
6614
0
1
66724
1.49871e-05
0
908
0
0
16508
0
1
121390
8.23791e-06
688564
chr6:24175018:A>C
DCDC2
NM_016356:p.Ile457Met
NM_016356:c.1371T>G
EXON10
Unknown significance
rs770029938
This variant is a VUS because it does not have enough information.
-0.438
N
0.006;0.003
D
0.745;0.989
P;D
0.151791
N
0.637256
N;N
2.83
C
1
10404
9.61169e-05
0
11576
0
0
8652
0
0
6614
0
0
66726
0
0
908
0
0
16510
0
1
121390
8.23791e-06
688565
chr6:24175021:T>A
DCDC2
NM_016356:p.Lys456Asn
NM_016356:c.1368A>T
EXON10
Benign
rs9460973
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
1.061
C
0.066;0.03
T;D
0.839;0.934
P
0.068137
N
0.999494
P;P
3.29
C
246
8600
0.0286047
1840
4406
0.417612
2086
13006
0.160388
654
1322
0.4947
25
1006
0.0249
38
694
0.0548
0
1008
0
0
978
0
717
5008
0.143171
4546
10402
0.437031
508
11576
0.0438839
1
8650
0.000115607
19
6614
0.00287269
1661
66726
0.0248928
28
908
0.030837
27
16510
0.00163537
6790
121386
0.0559373
688566
chr6:24175025:A>G
DCDC2
NM_016356:p.Val455Ala
NM_016356:c.1364T>C
EXON10
Unknown significance
rs763350514
This variant is a VUS because it does not have enough information.
1.199
C
0.0
D
0.993;1.0
D
0.005774
N
0.977657
D;D
5.67
C
0
10400
0
0
11576
0
6
8650
0.000693642
0
6614
0
0
66722
0
0
908
0
0
16510
0
6
121380
4.94315e-05
688567
chr6:24175030:T>C
DCDC2
NM_016356:p.Pro453Pro
NM_016356:c.1359A>G
EXON10
Unknown significance
rs374448795
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
10398
0
3
11576
0.000259157
1
8648
0.000115634
0
6614
0
5
66720
7.494e-05
0
908
0
5
16510
0.000302847
14
121374
0.000115346
688568
chr6:24175034:C>T
DCDC2
NM_016356:p.Arg452Lys
NM_016356:c.1355G>A
EXON10
Likely benign
rs745504901
Pathogenicity is based on prediction data only. 1 out of 6 predictions were pathogenic.
0.935
N
0.212;0.113
T
0.009;0.197
B
0.022876
N
0.931831
N;N
4.75
C
0
10396
0
0
11576
0
0
8650
0
0
6614
0
6
66720
8.99281e-05
0
908
0
0
16510
0
6
121374
4.9434e-05
688569
chr6:24175045:T>C
DCDC2
NM_016356:p.Gln448Gln
NM_016356:c.1344A>G
EXON10
Unknown significance
rs368603558
This variant is a VUS because it does not have enough information.
0
8600
0
2
4406
0.000453926
2
13006
0.000153775
1
10388
9.62649e-05
0
11574
0
0
8648
0
0
6614
0
0
66710
0
0
908
0
0
16510
0
1
121352
8.24049e-06
688570
chr6:24175049:G>A
DCDC2
NM_016356:p.Pro447Leu
NM_016356:c.1340C>T
EXON10
Unknown significance
rs767844134
This variant is a VUS because it does not have enough information.
0.097
N
0.403;0.09
T
0.244;0.992
B;D
0.17188
N
0.800135
D;D
4.79
C
0
10382
0
0
11568
0
0
8648
0
0
6614
0
0
66708
0
1
908
0.00110132
0
16508
0
1
121336
8.24158e-06
688571
chr6:24175055:A>G
DCDC2
NM_016356:p.Val445Ala
NM_016356:c.1334T>C
EXON10
Unknown significance
rs753419903
This variant is a VUS because it does not have enough information.
1.199
C
0.106;0.142
T
0.003;0.015
B
0.042338
N
1
D;D
0.235
C
0
10368
0
0
11572
0
0
8646
0
0
6614
0
1
66700
1.49925e-05
0
908
0
0
16504
0
1
121312
8.24321e-06
688572
chr6:24175057:A>C
DCDC2
NM_016356:p.Asp444Glu
NM_016356:c.1332T>G
EXON10
Likely benign
rs759063204
Pathogenicity is based on prediction data only. 0 out of 6 predictions were pathogenic.
-0.183
N
0.289;0.147
T
0.0;0.021
B
0.840244
N
1
N;N
-4.59
N
0
10360
0
0
11572
0
0
8646
0
0
6614
0
1
66698
1.4993e-05
0
908
0
0
16504
0
1
121302
8.24389e-06
688573
chr6:24175057:A>G
DCDC2
NM_016356:p.Asp444Asp
NM_016356:c.1332T>C
EXON10
Unknown significance
rs759063204
This variant is a VUS because it does not have enough information.
0
10360
0
0
11572
0
0
8646
0
0
6614
0
3
66698
4.49789e-05
0
908
0
0
16504
0
3
121302
2.47317e-05
688574
chr6:24175066:G>A
DCDC2
NM_016356:c.1327-4C>T
INTRON9
Unknown significance
rs372370231
This variant is a VUS because it does not have enough information.
0
10330
0
0
11566
0
0
8640
0
0
6614
0
1
66674
1.49984e-05
0
904
0
0
16490
0
1
121218
8.2496e-06
688575
chr6:24175066:G>T
DCDC2
NM_016356:c.1327-4C>A
INTRON9
Unknown significance
rs372370231
This variant is a VUS because it does not have enough information.
0
8600
0
1
4406
0.000226963
1
13006
7.68876e-05
688576
chr6:24175069:G>A
DCDC2
NM_016356:c.1327-7C>T
INTRON9
Unknown significance
rs758332744
This variant is a VUS because it does not have enough information.
0
10320
0
0
11564
0
0
8640
0
0
6612
0
2
66666
3.00003e-05
0
902
0
0
16492
0
2
121196
1.65022e-05
688577
chr6:24175071:A>G
DCDC2
NM_016356:c.1327-9T>C
INTRON9
Unknown significance
rs77929453
This variant is a VUS because it does not have enough information.
0
10304
0
0
11564
0
0
8638
0
0
6614
0
1
66646
1.50047e-05
0
902
0
0
16482
0
1
121150
8.25423e-06
688578
chr6:24175071:A>T
DCDC2
NM_016356:c.1327-9T>A
INTRON9
Unknown significance
rs77929453
This variant is a VUS because it does not have enough information.
688579
chr6:24175073:A>G
DCDC2
NM_016356:c.1327-11T>C
INTRON9
Unknown significance
rs751249656
This variant is a VUS because it does not have enough information.
0
10306
0
0
11560
0
0
8634
0
0
6614
0
2
66648
3.00084e-05
0
904
0
0
16480
0
2
121146
1.6509e-05
688580
chr6:24175074:T>C
DCDC2
NM_016356:c.1327-12A>G
INTRON9
Unknown significance
rs199507955
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
1
10306
9.70309e-05
1
11562
8.64902e-05
0
8636
0
0
6614
0
0
66648
0
0
904
0
0
16482
0
2
121152
1.65082e-05
688581
chr6:24175079:C>A
DCDC2
NM_016356:c.1327-17G>T
INTRON9
Unknown significance
rs780946244
This variant is a VUS because it does not have enough information.
0
10292
0
0
11554
0
0
8622
0
0
6614
0
0
66630
0
0
902
0
1
16476
6.06943e-05
1
121090
8.25832e-06
688582
chr6:24175084:C>A
DCDC2
NM_016356:c.1327-22G>T
INTRON9
Unknown significance
rs746009140
This variant is a VUS because it does not have enough information.
0
10264
0
0
11546
0
0
8604
0
0
6612
0
1
66568
1.50222e-05
0
900
0
0
16468
0
1
120962
8.26706e-06
688583
chr6:24175086:A>G
DCDC2
NM_016356:c.1327-24T>C
INTRON9
Unknown significance
rs769834353
This variant is a VUS because it does not have enough information.
0
10264
0
0
11550
0
0
8604
0
0
6612
0
1
66574
1.50209e-05
0
902
0
0
16474
0
1
120980
8.26583e-06
688584
chr6:24175089:G>T
DCDC2
NM_016356:c.1327-27C>A
INTRON9
Unknown significance
rs769203059
This variant is a VUS because it does not have enough information.
688585
chr6:24175099:G>C
DCDC2
NM_016356:c.1327-37C>G
INTRON9
Unknown significance
rs536228276
This variant is a VUS because it does not have enough information.
1
10178
9.82511e-05
0
11524
0
0
8554
0
0
6612
0
0
66502
0
0
900
0
0
16458
0
1
120728
8.28308e-06
688586
chr6:24175102:T>A
DCDC2
NM_016356:c.1327-40A>T
INTRON9
Unknown significance
rs537898800
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
0
10150
0
0
11514
0
0
8528
0
0
6606
0
0
66482
0
0
900
0
17
16440
0.00103406
17
120620
0.000140938
688587
chr6:24175102:T>G
DCDC2
NM_016356:c.1327-40A>C
INTRON9
Unknown significance
rs537898800
This variant is a VUS because it does not have enough information.
1
10150
9.85222e-05
0
11514
0
0
8528
0
0
6606
0
0
66482
0
0
900
0
0
16440
0
1
120620
8.2905e-06
688588
chr6:24175110:A>G
DCDC2
NM_016356:c.1327-48T>C
INTRON9
Unknown significance
rs774780884
This variant is a VUS because it does not have enough information.
0
9990
0
0
11486
0
1
8454
0.000118287
0
6598
0
0
66172
0
0
896
0
0
16422
0
1
120018
8.33208e-06
688589
chr6:24175121:C>T
DCDC2
NM_016356:c.1327-59G>A
INTRON9
Unknown significance
rs554387858
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
688590
chr6:24175124:T>C
DCDC2
NM_016356:c.1327-62A>G
INTRON9
Benign
rs3789219
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
218
1322
0.1649
163
1006
0.162
172
694
0.2478
580
1008
0.5754
265
978
0.271
1398
5008
0.279153
688591
chr6:24175138:T>C
DCDC2
NM_016356:c.1327-76A>G
INTRON9
Unknown significance
rs533734719
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
688592
chr6:24175142:T>C
DCDC2
NM_016356:c.1327-80A>G
INTRON9
Unknown significance
rs554040512
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
688593
chr6:24175186:C>T
DCDC2
NM_016356:c.1327-124G>A
INTRON9
Unknown significance
rs190393084
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
688594
chr6:24175207:T>C
DCDC2
NM_016356:c.1327-145A>G
INTRON9
Unknown significance
rs9379647
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
688595
chr6:24175222:C>T
DCDC2
NM_016356:c.1327-160G>A
INTRON9
Unknown significance
rs556557105
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
688596
chr6:24175296:C>T
DCDC2
NM_016356:c.1327-234G>A
INTRON9
Unknown significance
rs182269258
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
688597
chr6:24175297:C>T
DCDC2
NM_016356:c.1327-235G>A
INTRON9
Unknown significance
rs542273660
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
688598
chr6:24175306:T>C
DCDC2
NM_016356:c.1327-244A>G
INTRON9
Unknown significance
rs746867470
This variant is a VUS because it does not have enough information.
688599
chr6:24175319:A>G
DCDC2
NM_016356:c.1327-257T>C
INTRON9
Benign
rs6907583
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
138
1322
0.1044
1
1006
0.001
13
694
0.0187
0
1008
0
0
978
0
152
5008
0.0303514
688600
chr6:24175323:TTTA>-
DCDC2
NM_016356:c.1327-261_1327-256delTAAA
INTRON9
Benign
rs112382215
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
654
1322
0.4947
26
1006
0.0258
38
694
0.0548
0
1008
0
0
978
0
718
5008
0.143371
688601
chr6:24175341:T>C
DCDC2
NM_016356:c.1327-279A>G
INTRON9
Unknown significance
rs139881059
This variant is a VUS because it does not have enough information.
688602
chr6:24175380:C>G
DCDC2
NM_016356:c.1327-318G>C
INTRON9
Benign
rs16888787
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
47
1322
0.0356
8
1006
0.008
6
694
0.0086
0
1008
0
0
978
0
61
5008
0.0121805
688603
chr6:24175401:G>A
DCDC2
NM_016356:c.1327-339C>T
INTRON9
Unknown significance
rs541223430
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
688604
chr6:24175451:C>T
DCDC2
NM_016356:c.1327-389G>A
INTRON9
Unknown significance
rs761632871
This variant is a VUS because it does not have enough information.
688605
chr6:24175468:C>T
DCDC2
NM_016356:c.1327-406G>A
INTRON9
Unknown significance
rs767291950
This variant is a VUS because it does not have enough information.
688606
chr6:24175469:G>A
DCDC2
NM_016356:c.1327-407C>T
INTRON9
Unknown significance
rs754114630
This variant is a VUS because it does not have enough information.
688607
chr6:24175479:T>C
DCDC2
NM_016356:c.1327-417A>G
INTRON9
Benign
rs9467063
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
654
1322
0.4947
25
1006
0.0249
38
694
0.0548
0
1008
0
0
978
0
717
5008
0.143171
688608
chr6:24175502:C>A
DCDC2
NM_016356:c.1327-440G>T
INTRON9
Unknown significance
rs745825943
This variant is a VUS because it does not have enough information.
688609
chr6:24175528:T>C
DCDC2
NM_016356:c.1327-466A>G
INTRON9
Unknown significance
rs533404535
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
688610
chr6:24175532:A>C
DCDC2
NM_016356:c.1327-470T>G
INTRON9
Benign
rs76372805
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
40
1322
0.0303
0
1006
0
2
694
0.0029
0
1008
0
0
978
0
42
5008
0.00838658
688611
chr6:24175544:G>A
DCDC2
NM_016356:c.1327-482C>T
INTRON9
Benign
rs146676408
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
12
1008
0.0119
0
978
0
12
5008
0.00239617
688612
chr6:24175569:T>C
DCDC2
NM_016356:c.1327-507A>G
INTRON9
Benign
rs531226106
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
0
1322
0
6
1006
0.006
8
694
0.0115
13
1008
0.0129
0
978
0
27
5008
0.00539137
688613
chr6:24175605:T>A
DCDC2
NM_016356:c.1327-543A>T
INTRON9
Unknown significance
rs548204486
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
688614
chr6:24175621:C>T
DCDC2
NM_016356:c.1327-559G>A
INTRON9
Benign
rs74484539
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
1
1322
0.0008
20
1006
0.0199
9
694
0.013
2
1008
0.002
48
978
0.0491
80
5008
0.0159744
688615
chr6:24175632:G>A
DCDC2
NM_016356:c.1327-570C>T
INTRON9
Unknown significance
rs533938204
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
1
694
0.0014
1
1008
0.001
0
978
0
2
5008
0.000399361
688616
chr6:24175637:C>T
DCDC2
NM_016356:c.1327-575G>A
INTRON9
Unknown significance
rs149216263
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
688617
chr6:24175645:A>G
DCDC2
NM_016356:c.1327-583T>C
INTRON9
Benign
rs143418381
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
27
1322
0.0204
0
1006
0
3
694
0.0043
0
1008
0
0
978
0
30
5008
0.00599042
688618
chr6:24175718:C>A
DCDC2
NM_016356:c.1327-656G>T
INTRON9
Unknown significance
rs539699134
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
688619
chr6:24175722:A>G
DCDC2
NM_016356:c.1327-660T>C
INTRON9
Unknown significance
rs556520481
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
688620
chr6:24175744:G>C
DCDC2
NM_016356:c.1327-682C>G
INTRON9
Unknown significance
rs151288236
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
688621
chr6:24175781:C>T
DCDC2
NM_016356:c.1327-719G>A
INTRON9
Unknown significance
rs535458846
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
688622
chr6:24175816:G>T
DCDC2
NM_016356:c.1327-754C>A
INTRON9
Unknown significance
rs188285445
This variant is a VUS because it does not have enough information.
688623
chr6:24175822:G>C
DCDC2
NM_016356:c.1327-760C>G
INTRON9
Unknown significance
rs768417857
This variant is a VUS because it does not have enough information.
688624
chr6:24175835:C>T
DCDC2
NM_016356:c.1327-773G>A
INTRON9
Unknown significance
rs180752460
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
2
694
0.0029
0
1008
0
0
978
0
2
5008
0.000399361
688625
chr6:24175854:G>C
DCDC2
NM_016356:c.1327-792C>G
INTRON9
Unknown significance
rs185643606
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
688626
chr6:24175867:T>A
DCDC2
NM_016356:c.1327-805A>T
INTRON9
Benign
rs190062818
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
14
1322
0.0106
0
1006
0
0
694
0
0
1008
0
0
978
0
14
5008
0.00279553
688627
chr6:24175906:T>C
DCDC2
NM_016356:c.1327-844A>G
INTRON9
Benign
rs12174638
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
11
1322
0.0083
110
1006
0.1093
87
694
0.1254
184
1008
0.1825
148
978
0.1513
540
5008
0.107827
688628
chr6:24175916:T>A
DCDC2
NM_016356:c.1327-854A>T
INTRON9
Unknown significance
rs140558919
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
688629
chr6:24175929:T>C
DCDC2
NM_016356:c.1327-867A>G
INTRON9
Unknown significance
rs543672631
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
688630
chr6:24175959:G>A
DCDC2
NM_016356:c.1327-897C>T
INTRON9
Benign
rs150421561
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
2
694
0.0029
0
1008
0
0
978
0
11
5008
0.00219649
688631
chr6:24175960:C>T
DCDC2
NM_016356:c.1327-898G>A
INTRON9
Unknown significance
rs138371894
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
688632
chr6:24175969:A>C
DCDC2
NM_016356:c.1327-907T>G
INTRON9
Benign
rs78094593
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
97
1322
0.0734
5
1006
0.005
7
694
0.0101
0
1008
0
0
978
0
109
5008
0.0217652
688633
chr6:24175979:C>T
DCDC2
NM_016356:c.1327-917G>A
INTRON9
Unknown significance
rs561767177
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
688634
chr6:24175987:A>T
DCDC2
NM_016356:c.1327-925T>A
INTRON9
Unknown significance
rs530138146
This variant is a VUS because it does not have enough information.
688635
chr6:24175996:C>A
DCDC2
NM_016356:c.1327-934G>T
INTRON9
Unknown significance
rs778385676
This variant is a VUS because it does not have enough information.
688636
chr6:24175998:C>T
DCDC2
NM_016356:c.1327-936G>A
INTRON9
Unknown significance
rs527355987
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
688637
chr6:24175999:G>A
DCDC2
NM_016356:c.1327-937C>T
INTRON9
Unknown significance
rs765642368
This variant is a VUS because it does not have enough information.
688638
chr6:24176019:ATTTT>-
DCDC2
NM_016356:c.1327-957_1327-951delAAAAT
INTRON9
Benign
rs141128175
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
10
1322
0.0076
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
11
5008
0.00219649
688639
chr6:24176043:G>T
DCDC2
NM_016356:c.1327-981C>A
INTRON9
Unknown significance
rs547518651
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
688640
chr6:24176055:T>C
DCDC2
NM_016356:c.1327-993A>G
INTRON9
Unknown significance
rs752880535
This variant is a VUS because it does not have enough information.
688641
chr6:24176089:G>T
DCDC2
NM_016356:c.1327-1027C>A
INTRON9
Unknown significance
rs541779604
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
688642
chr6:24176104:C>T
DCDC2
NM_016356:c.1327-1042G>A
INTRON9
Unknown significance
rs777937740
This variant is a VUS because it does not have enough information.
688643
chr6:24176105:G>A
DCDC2
NM_016356:c.1327-1043C>T
INTRON9
Benign
rs181745699
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
27
1322
0.0204
0
1006
0
3
694
0.0043
1
1008
0.001
0
978
0
31
5008
0.0061901
688644
chr6:24176120:T>C
DCDC2
NM_016356:c.1327-1058A>G
INTRON9
Benign
rs375673509
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
688645
chr6:24176126:T>C
DCDC2
NM_016356:c.1327-1064A>G
INTRON9
Unknown significance
rs569847921
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
688646
chr6:24176130:A>T
DCDC2
NM_016356:c.1327-1068T>A
INTRON9
Unknown significance
rs747513521
This variant is a VUS because it does not have enough information.
688647
chr6:24176132:T>C
DCDC2
NM_016356:c.1327-1070A>G
INTRON9
Unknown significance
rs757756255
This variant is a VUS because it does not have enough information.
688648
chr6:24176163:T>C
DCDC2
NM_016356:c.1327-1101A>G
INTRON9
Unknown significance
rs781642676
This variant is a VUS because it does not have enough information.
688649
chr6:24176173:T>A
DCDC2
NM_016356:c.1327-1111A>T
INTRON9
Benign
rs4549612
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
520
1322
0.3933
811
1006
0.8062
566
694
0.8156
980
1008
0.9722
865
978
0.8845
3742
5008
0.747204
688650
chr6:24176200:C>A
DCDC2
NM_016356:c.1327-1138G>T
INTRON9
Unknown significance
rs555431545
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
688651
chr6:24176215:T>C
DCDC2
NM_016356:c.1327-1153A>G
INTRON9
Unknown significance
rs533240565
This variant is a VUS because it does not have enough information.
688652
chr6:24176216:G>T
DCDC2
NM_016356:c.1327-1154C>A
INTRON9
Unknown significance
rs186786694
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
688653
chr6:24176242:C>T
DCDC2
NM_016356:c.1327-1180G>A
INTRON9
Unknown significance
rs534764895
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
688654
chr6:24176243:G>A
DCDC2
NM_016356:c.1327-1181C>T
INTRON9
Unknown significance
rs769825010
This variant is a VUS because it does not have enough information.
688655
chr6:24176259:G>T
DCDC2
NM_016356:c.1327-1197C>A
INTRON9
Unknown significance
rs557843506
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
688656
chr6:24176279:GA>-
DCDC2
NM_016356:c.1327-1217_1327-1214delTC
INTRON9
Unknown significance
rs779453381
This variant is a VUS because it does not have enough information.
688657
chr6:24176299:T>C
DCDC2
NM_016356:c.1327-1237A>G
INTRON9
Benign
rs143930971
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
2
694
0.0029
0
1008
0
0
978
0
7
5008
0.00139776
688658
chr6:24176320:A>C
DCDC2
NM_016356:c.1327-1258T>G
INTRON9
Unknown significance
rs749178234
This variant is a VUS because it does not have enough information.
688659
chr6:24176356:C>T
DCDC2
NM_016356:c.1327-1294G>A
INTRON9
Unknown significance
rs543589707
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
688660
chr6:24176386:G>T
DCDC2
NM_016356:c.1327-1324C>A
INTRON9
Unknown significance
rs557582558
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
688661
chr6:24176417:A>T
DCDC2
NM_016356:c.1327-1355T>A
INTRON9
Unknown significance
rs146348254
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
688662
chr6:24176435:G>T
DCDC2
NM_016356:c.1327-1373C>A
INTRON9
Unknown significance
rs543315918
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
688663
chr6:24176448:C>G
DCDC2
NM_016356:c.1327-1386G>C
INTRON9
Unknown significance
rs561479193
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
688664
chr6:24176449:G>A
DCDC2
NM_016356:c.1327-1387C>T
INTRON9
Unknown significance
rs527306114
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
688665
chr6:24176468:G>A
DCDC2
NM_016356:c.1327-1406C>T
INTRON9
Unknown significance
rs545128274
This variant is a VUS because it does not have enough information.
688666
chr6:24176480:C>T
DCDC2
NM_016356:c.1327-1418G>A
INTRON9
Unknown significance
rs773800385
This variant is a VUS because it does not have enough information.
688667
chr6:24176481:G>A
DCDC2
NM_016356:c.1327-1419C>T
INTRON9
Unknown significance
rs761483545
This variant is a VUS because it does not have enough information.
688668
chr6:24176488:A>G
DCDC2
NM_016356:c.1327-1426T>C
INTRON9
Unknown significance
rs571485192
This variant is a VUS because it does not have enough information.
688669
chr6:24176502:T>C
DCDC2
NM_016356:c.1327-1440A>G
INTRON9
Unknown significance
rs370789579
This variant is a VUS because it does not have enough information.
688670
chr6:24176503:A>G
DCDC2
NM_016356:c.1327-1441T>C
INTRON9
Benign
rs77843782
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
1
1322
0.0008
6
1006
0.006
1
694
0.0014
0
1008
0
0
978
0
8
5008
0.00159744
688671
chr6:24176513:G>C
DCDC2
NM_016356:c.1327-1451C>G
INTRON9
Unknown significance
rs777031316
This variant is a VUS because it does not have enough information.
688672
chr6:24176518:T>G
DCDC2
NM_016356:c.1327-1456A>C
INTRON9
Unknown significance
rs759808369
This variant is a VUS because it does not have enough information.
688673
chr6:24176524:A>-
DCDC2
NM_016356:c.1327-1462delT
INTRON9
Benign
rs573726491
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
46
1322
0.0348
1
1006
0.001
2
694
0.0029
0
1008
0
1
978
0.001
50
5008
0.00998403
688674
chr6:24176555:A>-
DCDC2
NM_016356:c.1327-1493delT
INTRON9
Benign
rs34673398
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
523
1322
0.3956
810
1006
0.8052
563
694
0.8112
976
1008
0.9683
856
978
0.8753
3728
5008
0.744409
688675
chr6:24176555:A>C
DCDC2
NM_016356:c.1327-1493T>G
INTRON9
Unknown significance
rs76920301
This variant is a VUS because it does not have enough information.
688676
chr6:24176580:C>T
DCDC2
NM_016356:c.1327-1518G>A
INTRON9
Unknown significance
rs565723978
This variant is a VUS because it does not have enough information.
688677
chr6:24176589:T>C
DCDC2
NM_016356:c.1327-1527A>G
INTRON9
Unknown significance
rs564146218
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
688678
chr6:24176594:T>C
DCDC2
NM_016356:c.1327-1532A>G
INTRON9
Benign
rs10946681
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
520
1322
0.3933
813
1006
0.8082
566
694
0.8156
980
1008
0.9722
865
978
0.8845
3744
5008
0.747604
688679
chr6:24176638:T>C
DCDC2
NM_016356:c.1327-1576A>G
INTRON9
Unknown significance
rs549700496
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
688680
chr6:24176645:T>-
DCDC2
NM_016356:c.1327-1583delA
INTRON9
Benign
rs144420339
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
91
1322
0.0688
2
1006
0.002
6
694
0.0086
0
1008
0
0
978
0
99
5008
0.0197684
688681
chr6:24176656:T>C
DCDC2
NM_016356:c.1327-1594A>G
INTRON9
Unknown significance
rs569842418
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
688682
chr6:24176666:G>A
DCDC2
NM_016356:c.1327-1604C>T
INTRON9
Unknown significance
rs528306474
This variant is a VUS because it does not have enough information.
688683
chr6:24176681:A>G
DCDC2
NM_016356:c.1327-1619T>C
INTRON9
Benign
rs139083640
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
11
1322
0.0083
0
1006
0
0
694
0
0
1008
0
0
978
0
11
5008
0.00219649
688684
chr6:24176705:->A
DCDC2
NM_016356:c.1327-1643_1327-1642insT
INTRON9
Benign
rs35946558
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
179
1322
0.1354
265
1006
0.2634
250
694
0.3602
746
1008
0.7401
401
978
0.41
1841
5008
0.367612
688685
chr6:24176719:T>G
DCDC2
NM_016356:c.1327-1657A>C
INTRON9
Benign
rs16888803
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
332
1322
0.2511
21
1006
0.0209
25
694
0.036
0
1008
0
0
978
0
378
5008
0.0754792
688686
chr6:24176729:T>A
DCDC2
NM_016356:c.1327-1667A>T
INTRON9
Unknown significance
rs757596667
This variant is a VUS because it does not have enough information.
688687
chr6:24176735:A>G
DCDC2
NM_016356:c.1327-1673T>C
INTRON9
Unknown significance
rs565898772
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
688688
chr6:24176747:T>G
DCDC2
NM_016356:c.1327-1685A>C
INTRON9
Benign
rs10946682
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
210
1322
0.1589
273
1006
0.2714
258
694
0.3718
762
1008
0.756
412
978
0.4213
1915
5008
0.382388
688689
chr6:24176751:T>C
DCDC2
NM_016356:c.1327-1689A>G
INTRON9
Benign
rs10946683
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
521
1322
0.3941
813
1006
0.8082
566
694
0.8156
980
1008
0.9722
864
978
0.8834
3744
5008
0.747604
688691
chr6:24176753:T>A
DCDC2
NM_016356:c.1327-1691A>T
INTRON9
Unknown significance
rs9467064
This variant is a VUS because it does not have enough information.
688690
chr6:24176753:T>C
DCDC2
NM_016356:c.1327-1691A>G
INTRON9
Benign
rs9467064
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.