Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs2395029 0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02 12
rs10484554 0.807 0.200 6 31306778 intron variant C/T snv 0.12 11