ENG, endoglin, 2022

N. diseases: 371; N. variants: 114
Disease: Spontaneous, recurrent epistaxis ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554809253
rs1554809253
Entrez Id: 2022;102723566
Gene Symbol: ENG;LOC102723566
ENG;LOC102723566
CUI: C3809715
Disease:
Spontaneous, recurrent epistaxis 		C 0.700 CausalMutation CLINVAR