Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs1143623 0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs670 0.763 0.360 11 116837697 5 prime UTR variant C/T snv 0.17 13
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
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
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1803274 0.763 0.360 3 165773492 missense variant C/T snv 0.18 0.18 13
rs1126680 0.851 0.160 3 165837337 synonymous variant C/T snv 5.6E-02 5.6E-02 5
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs8192678 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs3732378 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48