Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2074755 0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 17
rs13244268 0.925 0.120 7 73497513 intron variant T/C snv 9.2E-02 2
rs7811265 0.925 0.120 7 73520180 intron variant A/G snv 0.23 2