RS797045950 SELENON

Health Risk Chr 1:25809104
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What This Variant Does
"CLNSIG=4
Associated Conditions
Congenital myopathy with fiber type disproportion
Eichsfeld type congenital muscular dystrophy
Congenital myopathy 4A
autosomal dominant
Congenital myopathy with fiber type disproportion
Eichsfeld type congenital muscular dystrophy
Congenital myopathy 4A
autosomal dominant
Other Variants in SELENON
rs121908182 rs587776597 rs121908184 rs121908185 rs121908186 rs368104077 rs121908187 rs121908188 rs398124359 rs377215510
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