TTR Chromosome 18

Transthyretin
122 variants 122 Health Risk

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What This Gene Does
This gene encodes one of the three prealbumins, which include alpha-1-antitrypsin, transthyretin and orosomucoid. The encoded protein, transthyretin, is a homo-tetrameric carrier protein, which transports thyroid hormones in the plasma and cerebrospinal fluid. It is also involved in the transport of retinol (vitamin A) in the plasma by associating with retinol-binding protein. The protein may also be involved in other intracellular processes including proteolysis, nerve regeneration, autophagy and glucose homeostasis. Mutations in this gene are associated with amyloid deposition, predominantly affecting peripheral nerves or the heart, while a small percentage of the gene mutations are non-amyloidogenic. The mutations are implicated in the etiology of several diseases, including amyloidotic polyneuropathy, euthyroid hyperthyroxinaemia, amyloidotic vitreous opacities, cardiomyopathy, oculoleptomeningeal amyloidosis, meningocerebrovascular amyloidosis and carpal tunnel syndrome. [provided by RefSeq, Aug 2017]
Gene Info
Gene Group
Gla domain containing
Locus Type
gene with protein product
Location
18q12.1
Ensembl
ENSG00000118271
Associated Conditions (19)
Cardiomyopathy
Amyloidosis
hereditary systemic 1
Cardiovascular phenotype
TTR-related disorder
Charcot-Marie-Tooth disease
Carpal tunnel syndrome 1
Hyperthyroxinemia
dystransthyretinemic
Hyperthyroidism
AMYLOIDOSIS
HEREDITARY SYSTEMIC 1
MODIFIER OF
Hypertrophic cardiomyopathy
Tip-toe gait
Carpal tunnel syndrome
Heart failure
Hereditary amyloidosis
ATTRV122I amyloidosis
Key Variants
RS112263266
Conflicting classifications of pathogenicity
Cardiomyopathy, Amyloidosis, hereditary systemic 1
Health Risk
RS11541793
Conflicting classifications of pathogenicity
Amyloidosis, hereditary systemic 1, Cardiovascular phenotype
Health Risk
RS11541797
Conflicting classifications of pathogenicity
Cardiovascular phenotype, Cardiomyopathy, Amyloidosis
Health Risk
RS121918095
Conflicting classifications of pathogenicity
Amyloidosis, hereditary systemic 1, Cardiovascular phenotype
Health Risk
RS138065384
Conflicting classifications of pathogenicity
Amyloidosis, hereditary systemic 1, Charcot-Marie-Tooth disease
Health Risk
RS138657343
Conflicting classifications of pathogenicity
Cardiovascular phenotype, Amyloidosis, hereditary systemic 1
Health Risk
RS143906738
Conflicting classifications of pathogenicity
Amyloidosis, hereditary systemic 1, Charcot-Marie-Tooth disease
Health Risk
RS145551875
Conflicting classifications of pathogenicity
Amyloidosis, hereditary systemic 1, Cardiovascular phenotype
Health Risk
RS1555631417
Conflicting classifications of pathogenicity
Amyloidosis, hereditary systemic 1, Cardiovascular phenotype
Health Risk
RS1567946170
Conflicting classifications of pathogenicity
Amyloidosis, hereditary systemic 1, Cardiovascular phenotype
Health Risk
RS2073510448
Conflicting classifications of pathogenicity
Amyloidosis, hereditary systemic 1, Cardiovascular phenotype
Health Risk
RS2073528142
Conflicting classifications of pathogenicity
Amyloidosis, hereditary systemic 1, Cardiovascular phenotype
Health Risk
All Variants (122)
RSID Category Clinical Significance Conditions
RS112263266 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Amyloidosis, hereditary systemic 1
RS11541793 Health Risk Conflicting classifications of pathogenicity Amyloidosis, hereditary systemic 1, Cardiovascular phenotype
RS11541797 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Cardiomyopathy, Amyloidosis
RS121918095 Health Risk Conflicting classifications of pathogenicity Amyloidosis, hereditary systemic 1, Cardiovascular phenotype
RS138065384 Health Risk Conflicting classifications of pathogenicity Amyloidosis, hereditary systemic 1, Charcot-Marie-Tooth disease
RS138657343 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Amyloidosis, hereditary systemic 1
RS143906738 Health Risk Conflicting classifications of pathogenicity Amyloidosis, hereditary systemic 1, Charcot-Marie-Tooth disease
RS145551875 Health Risk Conflicting classifications of pathogenicity Amyloidosis, hereditary systemic 1, Cardiovascular phenotype
RS1555631417 Health Risk Conflicting classifications of pathogenicity Amyloidosis, hereditary systemic 1, Cardiovascular phenotype
RS1567946170 Health Risk Conflicting classifications of pathogenicity Amyloidosis, hereditary systemic 1, Cardiovascular phenotype
RS2073510448 Health Risk Conflicting classifications of pathogenicity Amyloidosis, hereditary systemic 1, Cardiovascular phenotype
RS2073528142 Health Risk Conflicting classifications of pathogenicity Amyloidosis, hereditary systemic 1, Cardiovascular phenotype
RS2276382 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Amyloidosis, hereditary systemic 1
RS2510932394 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Amyloidosis, hereditary systemic 1
RS2510932395 Health Risk Conflicting classifications of pathogenicity Amyloidosis, hereditary systemic 1, Cardiovascular phenotype
RS267607159 Health Risk Conflicting classifications of pathogenicity Amyloidosis, hereditary systemic 1, Cardiovascular phenotype
RS28933981 Health Risk Conflicting classifications of pathogenicity AMYLOIDOSIS, HEREDITARY SYSTEMIC 1, MODIFIER OF
RS386134269 Health Risk Conflicting classifications of pathogenicity Amyloidosis, hereditary systemic 1, Amyloidosis
RS730881162 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Hyperthyroxinemia, dystransthyretinemic
RS730881164 Health Risk Conflicting classifications of pathogenicity Amyloidosis, hereditary systemic 1, Charcot-Marie-Tooth disease
RS730881165 Health Risk Conflicting classifications of pathogenicity Amyloidosis, hereditary systemic 1, Carpal tunnel syndrome 1
RS745422404 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Carpal tunnel syndrome 1, Amyloidosis
RS746692906 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Carpal tunnel syndrome 1, Amyloidosis
RS752579437 Health Risk Conflicting classifications of pathogenicity Amyloidosis, hereditary systemic 1, Cardiovascular phenotype
RS75517067 Health Risk Conflicting classifications of pathogenicity Amyloidosis, hereditary systemic 1, Charcot-Marie-Tooth disease
RS759512847 Health Risk Conflicting classifications of pathogenicity Amyloidosis, hereditary systemic 1, Cardiovascular phenotype
RS76410435 Health Risk Conflicting classifications of pathogenicity Amyloidosis, hereditary systemic 1, Charcot-Marie-Tooth disease
RS766223850 Health Risk Conflicting classifications of pathogenicity
RS769343676 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Cardiovascular phenotype
RS770389488 Health Risk Conflicting classifications of pathogenicity Amyloidosis, hereditary systemic 1, Carpal tunnel syndrome 1
RS773584864 Health Risk Conflicting classifications of pathogenicity Amyloidosis, hereditary systemic 1, Hyperthyroxinemia
RS774027595 Health Risk Conflicting classifications of pathogenicity Amyloidosis, hereditary systemic 1, Cardiovascular phenotype
RS781345808 Health Risk Conflicting classifications of pathogenicity Tip-toe gait, Tip-toe gait
RS876658108 Health Risk Conflicting classifications of pathogenicity Amyloidosis, hereditary systemic 1, Cardiovascular phenotype
RS915983905 Health Risk Conflicting classifications of pathogenicity Amyloidosis, hereditary systemic 1, Hyperthyroxinemia
RS933476040 Health Risk Conflicting classifications of pathogenicity Amyloidosis, hereditary systemic 1, Cardiovascular phenotype
RS967658213 Health Risk Conflicting classifications of pathogenicity Amyloidosis, hereditary systemic 1, Amyloidosis
RS104894664 Health Risk Likely pathogenic Amyloidosis, hereditary systemic 1, Cardiovascular phenotype
RS11541799 Health Risk Likely pathogenic Amyloidosis, hereditary systemic 1, Amyloidosis
RS121918073 Health Risk Likely pathogenic Amyloidosis, hereditary systemic 1, Cardiovascular phenotype
RS121918086 Health Risk Likely pathogenic Amyloidosis, hereditary systemic 1, Cardiovascular phenotype
RS121918087 Health Risk Likely pathogenic Amyloidosis, hereditary systemic 1, Amyloidosis
RS121918099 Health Risk Likely pathogenic Amyloidosis, hereditary systemic 1, Amyloidosis
RS1258875883 Health Risk Likely pathogenic Amyloidosis, hereditary systemic 1, Amyloidosis
RS1415606768 Health Risk Likely pathogenic Amyloidosis, hereditary systemic 1, Amyloidosis
RS1456101911 Health Risk Likely pathogenic Amyloidosis, hereditary systemic 1, Amyloidosis
RS1598845097 Health Risk Likely pathogenic Cardiovascular phenotype, Amyloidosis, hereditary systemic 1
RS2073510816 Health Risk Likely pathogenic Amyloidosis, hereditary systemic 1, Amyloidosis
RS2073511444 Health Risk Likely pathogenic Amyloidosis, hereditary systemic 1, Cardiovascular phenotype
RS2144406508 Health Risk Likely pathogenic Amyloidosis, hereditary systemic 1, Amyloidosis
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