Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs782596945
rs782596945
Entrez Id: 492
Gene Symbol: ATP2B3
ATP2B3
CUI: C0267071
Disease:
Oropharyngeal Dysphagia
T 0.700 CausalMutation CLINVAR