Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587783446
CHD7
0.763 0.280 8 60850546 stop gained C/T snv 19
rs1554603293
CHD7
0.752 0.320 8 60849154 missense variant G/A snv 17
rs387906271
CHD7
0.790 0.320 8 60801598 splice region variant G/C snv 11
rs121434341
CHD7
0.807 0.360 8 60855993 missense variant C/A;T snv 10
rs1563595095
CHD7
0.776 0.320 8 60781285 frameshift variant AA/T delins 10
rs1064793083
CHD7
0.882 0.080 8 60828682 missense variant C/T snv 4
rs1554602465
CHD7
0.882 0.080 8 60845063 missense variant G/A snv 4
rs121434344
CHD7
0.882 0.080 8 60816389 missense variant C/T snv 3
rs875989879
CHD7
0.925 0.080 8 60853017 stop gained C/T snv 3
rs886040988
CHD7
1.000 0.080 8 60830422 missense variant T/A snv 3
rs121434338
CHD7
0.925 0.080 8 60822627 missense variant A/G snv 2
rs121434343
CHD7
0.925 0.080 8 60853047 missense variant G/A snv 2
rs1563664506
CHD7
0.925 0.080 8 60856161 frameshift variant A/- del 2
rs200220845
CHD7
0.925 0.080 8 60822027 stop gained C/A;T snv 1.2E-05 2
rs200806228
CHD7
0.925 0.080 8 60853500 missense variant G/A snv 2.0E-04 1.5E-04 2
rs398124321
CHD7
0.925 0.080 8 60850486 splice region variant G/A;T snv 4.0E-06 2
rs587783450
CHD7
0.925 0.080 8 60852882 stop gained C/T snv 2
rs794727423
CHD7
0.925 0.080 8 60850476 intron variant G/A snv 2
rs886040983
CHD7
0.925 0.120 8 60822504 stop gained C/T snv 2
rs886040985
CHD7
0.925 0.080 8 60823843 stop gained C/T snv 2
rs886040991
CHD7
0.925 0.080 8 60838115 stop gained C/T snv 2
rs886040995
CHD7
1.000 0.080 8 60852682 stop gained C/T snv 2
rs1021645395
CHD7
1.000 0.080 8 60850497 stop gained T/C;G snv 3.5E-05 1
rs1057519423
CHD7
1.000 0.080 8 60742984 stop gained C/T snv 1
rs1057521077
CHD7
1.000 0.080 8 60822604 missense variant T/C snv 1