Disease: Myopathy ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894294
rs104894294
Entrez Id: 5913
Gene Symbol: RAPSN
RAPSN
CUI: C0026848
Disease:
Myopathy 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs104894299
rs104894299
Entrez Id: 5913
Gene Symbol: RAPSN
RAPSN
CUI: C0026848
Disease:
Myopathy 		T 0.700 GeneticVariation CLINVAR