RS121908188 SELENON
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What This Variant Does
"[OMIM:?]
Associated Conditions
Congenital myopathy with fiber type disproportion
Eichsfeld type congenital muscular dystrophy
SEPN1-related disorder
Congenital myopathy 4A
autosomal dominant
SELENON-related myopathy
Malignant tumor of esophagus
Inborn genetic diseases
Eichsfeld type congenital muscular dystrophy
Congenital myopathy with fiber type disproportion
Eichsfeld type congenital muscular dystrophy
SEPN1-related disorder
Congenital myopathy 4A
autosomal dominant
SELENON-related myopathy
GWAS Studies (1)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| Height | — | OR: 0.18 | 5E-11 | PubMed |
Other Variants in SELENON