RS199742668 SELENON

Health Risk Chr 1:25808592
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Associated Conditions
SEPN1-related disorder
Eichsfeld type congenital muscular dystrophy
SELENON-related disorder
Inborn genetic diseases
SEPN1-related disorder
Eichsfeld type congenital muscular dystrophy
SELENON-related disorder
Inborn genetic diseases
Other Variants in SELENON
rs121908182 rs587776597 rs121908184 rs121908185 rs121908186 rs368104077 rs121908187 rs121908188 rs398124359 rs377215510
Ask Dr. Hemsworth about this variant