Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs217181 16 72080103 intron variant C/T snv 0.20 6
rs1303 0.925 0.040 14 94378506 missense variant T/G snv 0.28 0.22 4