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 5
rs925946 0.882 0.120 11 27645655 intron variant T/G snv 0.72 3
rs11030104 0.790 0.240 11 27662970 intron variant A/G snv 0.16 2