Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 3
rs7904519 0.763 0.240 10 113014168 intron variant A/G snv 0.55 2
rs11196172 0.708 0.200 10 112967084 intron variant G/A snv 0.13 1
rs11196174 1.000 0.080 10 112974337 intron variant A/C;G snv 1
rs11196175 0.925 0.160 10 112976855 intron variant T/C snv 0.20 1
rs7900150 0.882 0.160 10 113034064 intron variant T/A;C snv 0.54 1