Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs121912438 0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs660118 0.807 0.080 11 65967703 missense variant G/C snv 0.46 0.36 6
rs1801320 0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12 15
rs786204929 0.752 0.200 10 87933144 stop gained G/A;T snv 12
rs3856806 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs587777790 0.732 0.280 3 179199690 missense variant G/A snv 14
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
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
rs4644 0.732 0.320 14 55138217 missense variant C/A;G snv 0.35 14
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62