Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3132946 0.882 0.240 6 32222251 intron variant A/G snv 0.91 3
rs422951 0.807 0.280 6 32220606 missense variant T/C snv 0.40 0.40 2
rs3131294 1.000 0.080 6 32212369 intron variant A/G snv 0.91 1
rs438475 1.000 0.080 6 32218468 intron variant G/A;C snv 1