Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 40
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 187
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 201
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 106
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 230
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 169
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 47
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 36
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 103
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 46
rs3856806 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 107
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 73
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193