Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs1273593548 0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82