Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4977756 0.683 0.440 9 22068653 intron variant G/A snv 0.64 24
rs121913503 0.689 0.200 15 90088606 missense variant C/A;T snv 23
rs6010620 0.701 0.360 20 63678486 intron variant A/C;G snv 21
rs1273593548 0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs1057519904 0.742 0.080 6 27872233 missense variant T/A snv 17
rs1057519902 0.742 0.160 1 226064451 missense variant G/C snv 16
rs11554137 0.742 0.040 2 208248468 synonymous variant G/A snv 5.1E-02 6.8E-02 13
rs371409680 0.790 0.120 17 7673772 missense variant C/G;T snv 4.0E-05 7.0E-06 10
rs149840192 0.807 0.080 7 55154129 missense variant C/A;T snv 7
rs374052197 0.882 0.040 1 13610421 missense variant G/A;T snv 8.0E-06 5
rs745934102 0.882 0.040 1 13607281 missense variant G/A snv 3.2E-05 1.4E-05 5
rs771563543 0.851 0.040 10 31510841 missense variant G/A snv 4.0E-06 1.4E-05 5