Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs140701 0.790 0.200 17 30211514 intron variant C/T snv 0.40 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