Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1800849 0.851 0.160 11 74009120 upstream gene variant G/A;T snv 5