Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12188300 0.807 0.120 5 159402519 intron variant A/G;T snv 6
rs4921482 0.807 0.120 5 159337470 intron variant T/C;G snv 6
rs74817271 0.807 0.120 5 151090412 intron variant G/A snv 5.0E-02 6
rs10865331 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 5
rs33980500 0.742 0.200 6 111592059 missense variant C/T snv 8.6E-02 9.7E-02 3
rs12191877 0.851 0.120 6 31285148 intron variant C/T snv 0.12 2
rs458017 0.925 0.080 6 111374888 missense variant T/C snv 5.9E-02 5.6E-02 2
rs702873 0.882 0.120 2 60854407 intron variant C/T snv 0.35 2