RS121918085 TTR
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What This Variant Does
"[OMIM:?]
Associated Conditions
Amyloidosis
hereditary systemic 1
Cardiovascular phenotype
Hyperthyroxinemia
dystransthyretinemic
Carpal tunnel syndrome 1
Amyloidosis
hereditary systemic 1
Cardiovascular phenotype
Hyperthyroxinemia
dystransthyretinemic
Carpal tunnel syndrome 1
Population Frequencies
gnomAD ALL
0%
Other Variants in TTR