Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
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
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1143623 0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1126680 0.851 0.160 3 165837337 synonymous variant C/T snv 5.6E-02 5.6E-02 5
rs1803274 0.763 0.360 3 165773492 missense variant C/T snv 0.18 0.18 13
rs3732378 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs8192678 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs8193036 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24