Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3746544 0.790 0.120 20 10306436 3 prime UTR variant G/T snv 0.68 10
rs3796863 0.790 0.160 4 15848363 intron variant G/T snv 0.41 8
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4141463 0.925 0.040 20 14766825 intron variant T/C snv 0.50 3
rs4307059 0.882 0.080 5 25967594 intron variant T/A;C snv 5
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs6150410 0.925 0.040 7 155454910 intron variant CGCATCCCC/-;CGCATCCCCCGCATCCCC delins 0.28 2
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs6735330 0.925 0.040 2 61504343 intron variant G/A snv 0.18 2
rs6950765 0.925 0.040 7 117281176 intron variant C/G snv 0.64 2
rs7294536 0.925 0.040 12 63154312 upstream gene variant T/C snv 0.26 2
rs736707 0.851 0.040 7 103489956 intron variant A/G snv 0.30 6
rs756472 0.925 0.040 16 14185624 intron variant G/A snv 0.24 2
rs7608798 0.925 0.040 2 162033707 intron variant G/A snv 0.35 2
rs768913131 0.925 0.040 2 50552821 missense variant G/A snv 3
rs7794745 0.851 0.040 7 146792514 intron variant A/T snv 0.49 6
rs779867 0.776 0.120 3 7442784 intron variant T/C;G snv 9
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs747756965 0.925 0.040 6 38775924 missense variant T/A;C snv 4.0E-06 2
rs73598374
ADA
0.790 0.280 20 44651586 missense variant C/A;G;T snv 7.1E-06; 6.2E-02 8
rs1800561 0.807 0.240 4 15824935 missense variant C/A;T snv 8.0E-06; 4.4E-04 7
rs751945904 0.925 0.040 X 5893158 missense variant G/A snv 1.1E-05 2
rs3747334 0.925 0.040 X 5893489 synonymous variant G/A;C;T snv 1.2E-05; 6.7E-03 3
rs362691 0.882 0.120 7 103610714 missense variant G/A;C;T snv 1.2E-05; 0.12 3
rs201551401 0.925 0.040 7 124746694 missense variant C/T snv 6.4E-05 1.4E-05 3