Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2287161 0.827 0.080 12 106987362 upstream gene variant C/G;T snv 7
rs10838524 0.851 0.120 11 45848626 intron variant A/G snv 0.42 5
rs11541353 0.851 0.120 2 100977729 missense variant C/T snv 0.14 0.14 4
rs2028122 0.851 0.120 15 60549076 intron variant A/G snv 0.51 4
rs2314339 0.851 0.120 17 40096959 intron variant C/T snv 0.20 4