Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2104286 0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs11465804 0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 10