Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs187115 0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs744166 0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs9651118 0.683 0.480 1 11802157 intron variant T/C snv 0.18 20
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs1051753269 0.790 0.120 7 55174029 missense variant G/A snv 7.0E-06 7
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
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
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121913227 0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33
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