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
rs12043259 1 204858913 intron variant C/G snv 0.11 2
rs2377339 2 105840835 intron variant A/G snv 4.8E-02 2