ENG, endoglin, 2022

N. diseases: 371; N. variants: 114
Disease: Telangiectasia, Hereditary Hemorrhagic, Type 1 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs878853659
rs878853659
Entrez Id: 2022
Gene Symbol: ENG
ENG
CUI: C4551861
Disease:
Telangiectasia, Hereditary Hemorrhagic, Type 1 		T 0.700 GeneticVariation CLINVAR