Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 107
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 169
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 40
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 83
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs3856806 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 47
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 46
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 73
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
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
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 484
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs11196067 0.752 0.160 10 112709306 intron variant A/T snv 0.32 10
rs16906252 0.732 0.200 10 129467281 synonymous variant C/T snv 5.5E-02 5.1E-02 17
rs562015640 0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 15
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 187
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 135
rs121918464 0.708 0.440 12 112450406 missense variant G/A;C snv 19