Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs5029939 0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs1050501 0.732 0.440 1 161674008 missense variant T/C snv 0.16 0.19 15