Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs4676410 0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 12
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 11
rs3024493 0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 7
rs11117431 0.807 0.160 16 85981710 intron variant A/G snv 0.18 6
rs1267499 0.807 0.160 6 14715651 intron variant T/A;C snv 6