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 93
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs7094871 1.000 0.080 10 112952395 intron variant C/G;T snv 1