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 8
rs11030104 0.790 0.240 11 27662970 intron variant A/G snv 0.16 4
rs7103411 0.752 0.160 11 27678578 intron variant C/T snv 0.82 3