RS121918074 TTR

Health Risk Chr 18:31595247
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What This Variant Does
"[OMIM:?]
Associated Conditions
Amyloidosis
hereditary systemic 1
Cardiovascular phenotype
Heart failure
Cardiomyopathy
Charcot-Marie-Tooth disease
Amyloidosis
hereditary systemic 1
Cardiovascular phenotype
Amyloidosis
hereditary systemic 1
Cardiovascular phenotype
Heart failure
Cardiomyopathy
Charcot-Marie-Tooth disease
Other Variants in TTR
rs28933979 rs121918068 rs121918075 rs121918069 rs121918070 rs121918071 rs121918072 rs121918073 rs76992529 rs11541796
Ask Dr. Hemsworth about this variant