Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11671784 0.790 0.240 19 13836482 non coding transcript exon variant G/A snv 1.2E-02 1.2E-02 9
rs11685387 0.776 0.240 2 216109091 splice region variant C/T snv 0.30 9
rs11871756 0.882 0.120 17 72730105 intron variant C/G snv 0.11 3
rs11892031 0.882 0.120 2 233656637 intron variant A/C;T snv 5
rs1189516787 0.882 0.120 19 33301681 missense variant C/G snv 7.1E-06 3
rs1194611372 0.763 0.320 1 152032679 missense variant A/C snv 9
rs1203030830 0.882 0.120 7 55155873 synonymous variant T/C snv 4.0E-06 3
rs1208415127 0.827 0.160 3 50331654 missense variant G/A snv 4.0E-06 6
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs121434629 0.763 0.320 7 6005918 missense variant C/A;T snv 1.6E-04; 8.1E-06 13
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121909218 0.672 0.360 10 87933145 missense variant G/A snv 25
rs121913105 0.653 0.600 4 1806163 missense variant A/C;T snv 30
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913479 0.763 0.280 4 1804362 missense variant G/A;T snv 4.0E-06 10
rs121913482 0.630 0.680 4 1801837 missense variant C/T snv 45
rs121913483 0.649 0.560 4 1801841 missense variant C/A;G;T snv 4.2E-06; 1.3E-05 31
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs12529 0.776 0.280 10 5094459 missense variant C/G snv 0.50 0.45 10
rs125701 0.790 0.160 3 9748794 upstream gene variant G/A snv 0.13 7
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs12628 0.776 0.160 11 534242 synonymous variant A/G snv 0.32 0.34 10
rs12683422 0.742 0.240 9 27969442 intron variant C/T snv 5.7E-02 11
rs1287276985 0.790 0.200 6 43782020 missense variant T/A;C snv 4.0E-06; 4.0E-06 7.0E-06 7