SELENON, selenoprotein N, 57190

N. diseases: 147; N. variants: 30
Disease: Myopathy ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908188
rs121908188
Entrez Id: 57190
Gene Symbol: SELENON
SELENON
CUI: C0026848
Disease:
Myopathy 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs199564797
rs199564797
Entrez Id: 57190
Gene Symbol: SELENON
SELENON
CUI: C0026848
Disease:
Myopathy 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs745886248
rs745886248
Entrez Id: 57190
Gene Symbol: SELENON
SELENON
CUI: C0026848
Disease:
Myopathy 		A 0.700 GeneticVariation CLINVAR