Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs568408 0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16 29
rs9808753 0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18 17
rs1494555 0.790 0.120 5 35871088 missense variant G/A snv 0.64 0.72 8
rs1439112 0.851 0.160 2 134305027 intron variant G/A snv 0.61 4
rs2777899 0.851 0.160 17 59755030 intron variant T/A;G snv 4