Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913667
rs121913667
Entrez Id: 4613;10408
Gene Symbol: MYCN;MYCNOS
MYCN;MYCNOS
CUI: C0796068
Disease:
Oculodigitoesophagoduodenal syndrome
A 0.700 CausalMutation CLINVAR