Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267606780
rs267606780
Entrez Id: 1910
Gene Symbol: EDNRB
EDNRB
CUI: C1838564
Disease:
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 2
A 0.700 SusceptibilityMutation CLINVAR