Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113547729 1.000 0.080 17 4121530 intron variant G/A snv 3.2E-02 1
rs7224685 1.000 0.080 17 4111090 intron variant G/T snv 0.32 1
rs781831 1.000 0.080 17 4044350 missense variant T/C snv 0.45 0.53 1
rs781852 1.000 0.080 17 4049808 missense variant A/G snv 0.41 0.50 1
rs8068804 1.000 0.080 17 4082570 intron variant G/A snv 0.35 1