Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs927772349
rs927772349
Entrez Id: 2050
Gene Symbol: EPHB4
EPHB4
CUI: C4748670
Disease:
CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION 2
T 0.700 CausalMutation CLINVAR
dbSNP: rs927772349
rs927772349
Entrez Id: 2050
Gene Symbol: EPHB4
EPHB4
CUI: C4748670
Disease:
CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION 2
A 0.700 CausalMutation CLINVAR