Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79105258 12 111280427 intron variant C/A;T snv 24
rs113918189 12 94325241 intron variant C/T snv 6.9E-02 2
rs2984348 X 72308510 intron variant C/T snv 0.31 2
rs35397826 17 68273941 missense variant A/G snv 0.12 0.11 2
rs7113624 11 87508051 regulatory region variant G/A;C snv 2