Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs121912660 0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs1273593548 0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19