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
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs1881457 0.790 0.280 5 132656717 intron variant A/C snv 0.21 9
rs848 0.807 0.240 5 132660808 3 prime UTR variant A/C snv 0.67 8
rs1295685 0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 7
rs1295686 0.882 0.160 5 132660151 intron variant T/A;C snv 0.68 7
rs115008099 1.000 0.080 5 132656189 intron variant C/T snv 0.15 2