Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7811265 0.925 0.120 7 73520180 intron variant A/G snv 0.23 5
rs2074755 0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 4
rs13244268 0.925 0.120 7 73497513 intron variant T/C snv 9.2E-02 3
rs10239940 7 73487060 intron variant A/T snv 2.6E-02 2