Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1805127 0.732 0.240 21 34449523 missense variant T/C snv 0.64 2.0E-04 17
rs120074192 0.763 0.120 11 2527959 missense variant A/G snv 10
rs3745297
HRC
0.790 0.120 19 49154952 missense variant A/C snv 0.41 0.38 10
rs7626962 0.790 0.080 3 38579416 missense variant G/A;T snv 1.6E-05; 5.9E-03 10
rs104894503 0.776 0.160 15 63060899 missense variant G/A snv 1.6E-05 2.8E-05 9
rs3766871 0.790 0.240 1 237614784 missense variant G/A;T snv 4.0E-02 9
rs794728708 0.827 0.120 1 237377386 missense variant G/A;T snv 8
rs199473605 0.851 0.120 3 38560374 missense variant C/G;T snv 4.8E-05; 4.0E-06 7
rs104894584 0.851 0.120 17 70175553 missense variant G/A snv 5
rs1860561 0.851 0.080 12 110345436 intron variant G/A snv 0.19 5
rs755373114 0.925 0.080 4 113341742 missense variant A/C snv 7.2E-05 3
rs1355262401 1.000 0.080 6 121447691 missense variant T/G snv 7.0E-06 2