Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3804329 1.000 0.080 6 106238552 intron variant A/G snv 0.15 2
rs62625308 0.851 0.200 17 43091924 stop gained G/A;C snv 1.2E-05 2
rs2336219 1.000 0.080 19 45409148 missense variant G/A snv 0.21 0.19 2
rs1156560901 2 201880120 missense variant A/G snv 1.4E-05 2
rs10420252 1.000 0.080 19 35648270 upstream gene variant G/A snv 9.7E-02 2
rs6510502 1.000 0.080 19 35647577 upstream gene variant A/C;G snv 2
rs723526 1.000 7 55067126 intron variant A/G snv 0.86 2
rs1308088661 17 39727880 missense variant G/A snv 4.0E-06 2
rs9397080 1.000 0.040 6 152059380 intron variant C/T snv 0.22 2
rs62054619 1.000 0.080 16 90029890 non coding transcript exon variant G/A snv 0.14 2
rs2286742 1.000 0.080 10 113580733 intron variant G/A;C snv 0.57; 8.2E-06 2
rs3740530 1.000 0.080 10 113574365 synonymous variant C/T snv 0.63 0.55 2
rs140451238
ITK
1.000 0.080 5 157208978 synonymous variant T/C snv 1.6E-04 7.8E-04 2
rs3923594 1.000 0.120 11 119317205 intron variant C/A;T snv 7.1E-06 2
rs181264737 8 124589710 missense variant C/A;G;T snv 1.2E-05; 4.1E-06; 4.1E-06 2
rs11246050 1.000 0.080 11 284257 synonymous variant G/A;C snv 0.16; 4.0E-06 2
rs1347591 1.000 0.080 16 56834788 intron variant A/G snv 0.47 0.47 2
rs4461062 1.000 0.080 16 56830706 intron variant C/T snv 0.48 0.48 2
rs367722824 1.000 0.120 4 54278512 missense variant G/A snv 8.0E-06 2.1E-05 2
rs771308693 8 140752306 missense variant G/A snv 3.2E-05 7.0E-06 2
rs2118593 1.000 0.080 3 72447740 upstream gene variant G/A;C;T snv 2
rs753066745 X 81277164 missense variant C/T snv 1.7E-05 9.5E-06 2
rs1410727652 1.000 0.080 6 160348669 missense variant C/T snv 7.0E-06 2
rs33954691 1.000 0.080 5 1255405 synonymous variant G/A snv 0.13 9.0E-02 2
rs992157 0.790 0.080 2 218290058 5 prime UTR variant G/A snv 0.46 2