ENG, endoglin, 2022

N. diseases: 371; N. variants: 114
Disease: Hereditary hemorrhagic telangiectasia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554810177
rs1554810177
Entrez Id: 2022;105379841
Gene Symbol: ENG;LOC105379841
ENG;LOC105379841
CUI: C0039445
Disease:
Hereditary hemorrhagic telangiectasia 		TC 0.700 CausalMutation CLINVAR