Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs73069940 1.000 0.080 4 1242714 intron variant C/G snv 0.11 1
rs72501962 1.000 0.080 4 1252250 non coding transcript exon variant A/T snv 9.4E-02 1
rs79407053 1.000 0.080 4 1250430 non coding transcript exon variant G/A snv 9.4E-02 1