Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913482 0.630 0.680 4 1801837 missense variant C/T snv 45
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042028 0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30