RS727504181 TPM3

Health Risk Chr 1:154172927
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What This Variant Does
"CLNSIG=5
Associated Conditions
Congenital myopathy 4B
autosomal recessive
Congenital myopathy with fiber type disproportion
TPM3-related myopathy
Congenital myopathy 4B
autosomal recessive
Congenital myopathy with fiber type disproportion
TPM3-related myopathy
Other Variants in TPM3
rs80358247 rs199474720 rs80358248 rs121964852 rs199474719 rs121964853 rs121964854 rs199474713 rs797046047 rs876661406
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