Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9771228 7 32282884 intron variant T/C snv 0.39 2
rs10236197 7 32252149 intron variant T/C snv 0.41 1
rs215600 7 32294030 intron variant G/A;C snv 1
rs9648380 7 32171821 intron variant A/G snv 0.44 1