Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894395
GJB2
1.000 0.120 13 20189352 stop gained C/T snv 4.0E-06 1
rs104894396
GJB2
0.672 0.400 13 20189511 stop gained C/T snv 5.8E-04 1.1E-04 28
rs104894397
GJB2
0.882 0.120 13 20189353 missense variant A/G snv 4.0E-05 1.1E-04 3
rs104894398
GJB2
0.776 0.280 13 20189443 stop gained C/A;T snv 1.3E-04; 4.0E-06 10
rs104894401
GJB2
0.851 0.120 13 20189154 missense variant C/T snv 4
rs104894402
GJB2
0.882 0.200 13 20189359 missense variant G/A;C snv 5
rs104894403
GJB2
0.851 0.240 13 20189386 missense variant C/A;G;T snv 4.0E-06 7
rs104894404
GJB2
0.882 0.200 13 20189406 missense variant C/G;T snv 4
rs104894406
GJB2
0.925 0.200 13 20188977 missense variant C/A snv 2
rs104894407
GJB2
0.925 0.120 13 20189450 stop gained C/G;T snv 2.8E-05 3
rs104894408
GJB2
0.742 0.280 13 20189548 missense variant C/A;G snv 5.1E-04 13
rs104894409
GJB2
0.827 0.120 13 20189332 missense variant C/A;G;T snv 1.6E-05; 3.6E-05; 4.0E-06 6
rs104894410
GJB2
0.807 0.320 13 20189407 missense variant C/G;T snv 6
rs104894412
GJB2
0.925 0.320 13 20189420 missense variant G/T snv 2
rs104894413
GJB2
0.776 0.280 13 20189451 stop gained C/G;T snv 2.4E-05 9
rs1057517491
GJB2
0.776 0.240 13 20189448 frameshift variant C/- delins 8
rs1057517508
GJB2
0.925 0.120 13 20189068 frameshift variant A/- del 2
rs1057517519
GJB2
0.925 0.120 13 20189523 missense variant A/G snv 3
rs1057517521
GJB2
0.925 0.120 13 20189006 frameshift variant TG/- delins 2
rs1064797088
GJB2
0.925 0.120 13 20189446 missense variant C/T snv 2
rs1064797089
GJB2
1.000 0.120 13 20189418 missense variant G/T snv 1
rs1064797090
GJB2
1.000 0.120 13 20189410 missense variant G/A;C snv 1
rs111033186
GJB2
1.000 0.120 13 20189125 missense variant C/T snv 9.3E-03 3.5E-03 1
rs111033190
GJB2
0.925 0.120 13 20189487 missense variant C/A;T snv 3.2E-05; 4.0E-06 3
rs111033196
GJB2
1.000 0.120 13 20189202 missense variant C/A;T snv 2.8E-04; 1.4E-02 2