RS121908185 SELENON

Health Risk Chr 1:25813890
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What This Variant Does
"[OMIM:?]
Associated Conditions
Eichsfeld type congenital muscular dystrophy
SEPN1-related disorder
Muscular dystrophy
Cleft lip/palate
Inborn genetic diseases
Eichsfeld type congenital muscular dystrophy
SEPN1-related disorder
Muscular dystrophy
Cleft lip/palate
Inborn genetic diseases
Other Variants in SELENON
rs121908182 rs587776597 rs121908184 rs121908186 rs368104077 rs121908187 rs121908188 rs398124359 rs377215510 rs149623434
Ask Dr. Hemsworth about this variant