RS138065384 TTR
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What This Variant Does
"CLNSIG=4
Associated Conditions
Amyloidosis
hereditary systemic 1
Charcot-Marie-Tooth disease
Cardiomyopathy
Cardiovascular phenotype
Carpal tunnel syndrome 1
Hyperthyroxinemia
dystransthyretinemic
Amyloidosis
hereditary systemic 1
Charcot-Marie-Tooth disease
Cardiomyopathy
Cardiovascular phenotype
Carpal tunnel syndrome 1
Hyperthyroxinemia
Other Variants in TTR