ENG, endoglin, 2022

N. diseases: 371; N. variants: 114
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1085307436
rs1085307436
Entrez Id: 2022;102723566
Gene Symbol: ENG;LOC102723566
ENG;LOC102723566
CUI: C4552070
Disease:
Pulmonary Hypertension, Primary, 1
A 0.700 CausalMutation CLINVAR Pulmonary Arterial Hypertension: A Current Perspective on Established and Emerging Molecular Genetic Defects. 26387786 2015