RS121964854 TPM3
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What This Variant Does
"[OMIM:?]
Associated Conditions
Congenital myopathy with fiber type disproportion
Congenital myopathy 4B
autosomal recessive
Congenital myopathy 4A
autosomal dominant
TPM3-related core myopathy
Congenital myopathy with fiber type disproportion
Congenital myopathy 4A
autosomal dominant
Congenital myopathy 4B
autosomal recessive
Inborn genetic diseases
Nemaline myopathy
Congenital myopathy with fiber type disproportion
Congenital myopathy 4B
Other Variants in TPM3