Disease: Neuromuscular dysphagia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1568523935
rs1568523935
Entrez Id: 284439
Gene Symbol: SLC25A42
SLC25A42
CUI: C4025729
Disease:
Neuromuscular dysphagia 		G 0.700 GeneticVariation CLINVAR