Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
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
rs121913483 0.649 0.560 4 1801841 missense variant C/A;G;T snv 4.2E-06; 1.3E-05 31
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
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs12921862 0.763 0.200 16 331927 intron variant C/A snv 0.18 10
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1322643228 0.807 0.280 12 104321110 missense variant C/T snv 7.1E-06 6
rs1323541164 1.000 0.120 9 132921834 missense variant A/C snv 1
rs1326656542 0.776 0.280 13 108210293 missense variant A/T snv 4.0E-06 10
rs13278062 0.807 0.200 8 23225458 non coding transcript exon variant G/A;C;T snv 8
rs1336331763 0.882 0.120 16 28606796 missense variant G/A snv 4.0E-06 3
rs138213197 0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 24