Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1044250 0.807 0.240 19 8371280 missense variant C/T snv 0.30 0.29 12
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
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
rs4969168 0.790 0.480 17 78357712 3 prime UTR variant A/G snv 0.71 7
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs2057482 0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
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
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs290487 0.776 0.280 10 113149972 intron variant C/T snv 0.16 10
rs11977021 0.827 0.240 7 106288069 upstream gene variant C/T snv 0.22 5
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs7799039 0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226