Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs372065719 7 49779038 intron variant -/GGAG delins 1
rs481076 7 49778721 intron variant T/C;G snv 1
rs482968 7 49778531 intron variant G/A snv 0.53 1
rs79259707 7 49772968 upstream gene variant C/A snv 0.11 1