Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121913255 0.667 0.400 1 114713907 missense variant T/A;G snv 26
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
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs121913283 0.724 0.440 3 179234286 missense variant G/A;T snv 4.0E-06 16
rs121913428 0.827 0.120 7 55174015 missense variant G/A;C snv 6
rs121913444 0.724 0.160 7 55191831 missense variant T/A;C;G snv 18
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs1273593548 0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs149840192 0.807 0.080 7 55154129 missense variant C/A;T snv 7
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
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