Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1800471 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs11554495 0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 19
rs1131445 0.724 0.440 15 81309441 3 prime UTR variant T/A;C snv 16
rs72613567 0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs2281135 0.851 0.160 22 43936690 intron variant G/A snv 0.19 10
rs626283 0.827 0.160 19 54173307 upstream gene variant C/G snv 0.61 7
rs9273349 0.827 0.200 6 32658092 upstream gene variant T/C;G snv 6
rs774062108 0.925 0.240 4 102607651 splice region variant T/G snv 4.0E-06 3
rs778338788 1.000 0.080 15 81300440 synonymous variant T/C snv 4.0E-06 2
rs3917328 1.000 0.080 2 102178081 3 prime UTR variant C/G;T snv 5.1E-02 2
rs4648143 1.000 0.080 4 102616617 3 prime UTR variant G/A;T snv 5.0E-03; 4.0E-06 2
rs1368439 1.000 0.080 5 159315006 3 prime UTR variant G/T snv 0.87 2
rs10433879 4 87309988 intron variant G/C snv 0.20 1