Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs41281081
MET
1.000 0.080 7 116796211 3 prime UTR variant G/A snv 2.5E-03 3
rs76322625
MET
1.000 0.080 7 116798111 3 prime UTR variant C/A;T snv 3
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1458974438 0.807 0.080 19 1206957 missense variant G/A snv 9
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs752021744 0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29
rs121913364 0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 34
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
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
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs11662595 0.882 0.120 18 24477006 missense variant A/G snv 8.6E-02 7.6E-02 7
rs61764370 0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs121913535 0.742 0.320 12 25245348 missense variant C/A;G;T snv 14
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144