Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801320 0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12 15
rs660118 0.807 0.080 11 65967703 missense variant G/C snv 0.46 0.36 6
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs78378222 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37