Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
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
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs1800588 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16