RS876661406 TPM3

Health Risk Chr 1:154170679
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What This Variant Does
"CLNSIG=5
Associated Conditions
Congenital myopathy 4A
autosomal dominant
Congenital myopathy 4A
autosomal dominant
Other Variants in TPM3
rs80358247 rs199474720 rs80358248 rs121964852 rs199474719 rs121964853 rs121964854 rs199474713 rs727504181 rs797046047
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