Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6950324 7 133369958 intron variant T/C;G snv 1
rs6972284 7 133850961 intron variant T/C snv 0.63 1
rs6973256 7 133370849 intron variant C/T snv 0.64 1