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
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs1800890 0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21
rs4245739 0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06 21
rs1256046734 0.763 0.280 1 65621409 missense variant A/G snv 7.0E-06 12
rs201765376
MTR
0.732 0.360 1 236838504 synonymous variant C/T snv 1.6E-05 1.4E-05 12
rs1052576 0.807 0.200 1 15506048 missense variant T/A;C snv 0.53 9
rs12711521 0.807 0.240 1 11030859 missense variant C/A snv 0.74 0.63 7
rs1353759920 0.851 0.120 1 3707593 missense variant C/A snv 2.1E-05 4
rs1041163 0.882 0.160 1 100718269 upstream gene variant T/C snv 0.18 3
rs121908689 0.925 0.120 1 46272758 missense variant T/A snv 2
rs207186 0.925 0.120 1 55359252 intron variant C/T snv 7.7E-03 2
rs4661636 0.925 0.160 1 15496566 intron variant C/T snv 0.24 2
rs61733010 0.925 0.120 1 45561805 missense variant C/G;T snv 4.0E-06; 4.3E-04 1.9E-03 2
rs1800893 1.000 0.120 1 206773822 intron variant C/T snv 0.41 1
rs766588452 1.000 0.120 1 65621389 missense variant A/C;G snv 8.0E-06; 2.0E-05 1
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115