Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs4149056 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs79105258 12 111280427 intron variant C/A;T snv 24
rs198851 6 26104404 downstream gene variant T/A;C;G snv 15