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
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
rs3219489 0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27 24
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs9651118 0.683 0.480 1 11802157 intron variant T/C snv 0.18 20
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs752021744 0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29
rs876658657 0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1051753269 0.790 0.120 7 55174029 missense variant G/A snv 7.0E-06 7
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913227 0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
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
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs28929495 0.807 0.120 7 55174014 missense variant G/A;C;T snv 9
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs909797662 0.790 0.120 7 55191837 missense variant G/A snv 8