Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2723064
rs2723064
LINC02245 ; LINC02576 ; LOC107984063
1.000 0.080 2 65052671 non coding transcript exon variant T/C snv 0.40
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.700 1.000 2 2017 2018
dbSNP: rs2540953
rs2540953
LINC02245 ; LINC02576 ; LOC107984063
1.000 0.080 2 65045228 intron variant G/A snv 0.60
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.700 1.000 1 2017 2017