Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2723064
LOC107984063 ; LINC02245 ; LINC02576
1.000 0.080 2 65052671 non coding transcript exon variant T/C snv 0.40 1
rs2540953
LOC107984063 ; LINC02576 ; LINC02245
1.000 0.080 2 65045228 intron variant G/A snv 0.60 1