Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1051931 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12413409 0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 9
rs1256049 0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 32
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs4746720 0.790 0.320 10 67917073 3 prime UTR variant T/C snv 2.4E-02 7