RS776738184 SELENON

Health Risk Chr 1:25809688
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What This Variant Does
"CLNSIG=4
Associated Conditions
SEPN1-related disorder
Eichsfeld type congenital muscular dystrophy
SEPN1-related disorder
Eichsfeld type congenital muscular dystrophy
Other Variants in SELENON
rs121908182 rs587776597 rs121908184 rs121908185 rs121908186 rs368104077 rs121908187 rs121908188 rs398124359 rs377215510
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