RAB5B, RAB5B, member RAS oncogene family, 5869

N. diseases: 22; N. variants: 10
Disease: Gastroesophageal reflux disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11171710
rs11171710
Entrez Id: 5869
Gene Symbol: RAB5B
RAB5B
CUI: C0017168
Disease:
Gastroesophageal reflux disease 		A 0.700 GeneticVariation GWASCAT Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases. 31527586 2019