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
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
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
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs6280 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53