Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1545843 0.827 0.120 12 84170289 intron variant G/A snv 0.52 6
rs1876828 0.851 0.160 17 45834159 intron variant C/T snv 0.14 4
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs2435200 0.925 0.080 17 45994485 intron variant G/A snv 0.40 5
rs40184 0.851 0.120 5 1394962 intron variant C/T snv 0.45 5
rs6438552 0.790 0.280 3 119912967 intron variant A/G snv 0.54 9
rs7225002 0.925 0.080 17 46111701 intron variant A/G snv 0.39 7
rs738499 0.851 0.120 22 41381096 intron variant G/T snv 0.76 9
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
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
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs749437638 0.752 0.240 22 19968597 missense variant C/T snv 2.4E-05 1.4E-05 14
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs1137070 0.763 0.160 X 43744144 synonymous variant T/C snv 0.62 9