Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10165200 2 8299499 intron variant G/A snv 0.36 2
rs13416555 1.000 0.080 2 8301605 intron variant C/A;G snv 2
rs346835 2 8298563 intron variant C/T snv 0.39 2