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
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs670 0.763 0.360 11 116837697 5 prime UTR variant C/T snv 0.17 13
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
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
rs1979277 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 45
rs4818 0.683 0.440 22 19963684 synonymous variant C/G;T snv 0.34 27
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
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800730 0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
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
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66