RS80358247 TPM3
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What This Variant Does
"[OMIM:?]
Associated Conditions
Congenital myopathy 4B
autosomal recessive
Congenital myopathy 4A
autosomal dominant
Congenital myopathy 4B
autosomal recessive
Congenital myopathy 4A
autosomal dominant
Other Variants in TPM3