Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 25
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs11042023 1.000 0.080 11 8640969 missense variant T/C snv 0.60 0.59 3
rs56356382 19 4064059 intron variant T/C snv 0.24 3