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: rs759191907
rs759191907
Entrez Id: 2022;105379841
Gene Symbol: ENG;LOC105379841
ENG;LOC105379841
CUI: C0013595
Disease:
Eczema
G 0.700 CausalMutation CLINVAR