Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs340005 15 60585831 intron variant G/A snv 0.67 3
rs340025 15 60616108 intron variant T/A;C snv 3
rs340029 15 60602766 intron variant C/T snv 0.70 1