RS886041584 SELENON

Health Risk Chr 1:25811533
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What This Variant Does
"CLNSIG=5
Associated Conditions
Congenital myopathy 4A
autosomal dominant
Congenital myopathy 4A
autosomal dominant
Other Variants in SELENON
rs121908182 rs587776597 rs121908184 rs121908185 rs121908186 rs368104077 rs121908187 rs121908188 rs398124359 rs377215510
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