Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs6897932 0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs9264942 0.763 0.400 6 31306603 intron variant T/C snv 0.34 15
rs179008 0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18 14
rs396991 0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14