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: rs7763910
rs7763910
Entrez Id: 11120;285819
Gene Symbol: BTN2A1;LOC285819
BTN2A1;LOC285819
CUI: C0017168
Disease:
Gastroesophageal reflux disease 		G 0.700 GeneticVariation GWASCAT Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases. 31527586 2019