RS80358248 TPM3
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What This Variant Does
"[OMIM:?]
Associated Conditions
Congenital myopathy 4B
autosomal recessive
Congenital myopathy with fiber type disproportion
Congenital myopathy 4A
autosomal dominant
Congenital myopathy 4B
autosomal recessive
Congenital myopathy with fiber type disproportion
Congenital myopathy 4A
autosomal dominant
Other Variants in TPM3