Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs1320702652 0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs1800777 0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs753152 0.882 0.160 17 42761487 intron variant T/G snv 0.12 6
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs2295490 0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88