RS730881168 TTR

Health Risk Chr 18:31595139
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What This Variant Does
"CLNSIG=4
Associated Conditions
Amyloidosis
hereditary systemic 1
Cardiovascular phenotype
Amyloidosis
hereditary systemic 1
Cardiovascular phenotype
Other Variants in TTR
rs28933979 rs121918068 rs121918075 rs121918069 rs121918070 rs121918071 rs121918072 rs121918073 rs76992529 rs121918074
Ask Dr. Hemsworth about this variant