ENG, endoglin, 2022

N. diseases: 371; N. variants: 114
Disease: Pulmonary Hypertension, Primary, 1 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs142896669
rs142896669
Entrez Id: 2022;102723566
Gene Symbol: ENG;LOC102723566
ENG;LOC102723566
CUI: C4552070
Disease:
Pulmonary Hypertension, Primary, 1 		T 0.700 CausalMutation CLINVAR Hemodynamic and genetic analysis in children with idiopathic, heritable, and congenital heart disease associated pulmonary arterial hypertension. 23298310 2013