rs1567945632
|
Entrez Id: |
7276 |
Gene Symbol: |
TTR |
TTR
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Asp58Ala is the predominant mutation of the TTR gene in Korean patients with hereditary transthyretin-related amyloidosis.
|
25644864 |
2015 |
rs1567945632
|
Entrez Id: |
7276 |
Gene Symbol: |
TTR |
TTR
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Amyloid fibrils containing fragmented ATTR may be the standard fibril composition in ATTR amyloidosis.
|
23713495 |
2013 |
rs1567945632
|
Entrez Id: |
7276 |
Gene Symbol: |
TTR |
TTR
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
A |
0.700 |
GeneticVariation |
CLINVAR |
A transthyretin variant, Asp18Asn, associated with amyloid cardiomyopathy: a new African-American variant?
|
23126592 |
2012 |
rs1567945632
|
Entrez Id: |
7276 |
Gene Symbol: |
TTR |
TTR
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Liver transplantation and combined liver-heart transplantation in patients with familial amyloid polyneuropathy: a single-center experience.
|
20209591 |
2010 |
rs1567945632
|
Entrez Id: |
7276 |
Gene Symbol: |
TTR |
TTR
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Genetic microheterogeneity of human transthyretin detected by IEF.
|
17503405 |
2007 |
rs1567945632
|
Entrez Id: |
7276 |
Gene Symbol: |
TTR |
TTR
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
A |
0.700 |
GeneticVariation |
CLINVAR |
The biological and chemical basis for tissue-selective amyloid disease.
|
15820680 |
2005 |
rs1567945632
|
Entrez Id: |
7276 |
Gene Symbol: |
TTR |
TTR
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Tabulation of human transthyretin (TTR) variants, 2003.
|
14640030 |
2003 |
rs1567945632
|
Entrez Id: |
7276 |
Gene Symbol: |
TTR |
TTR
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Meningocerebrovascular amyloidosis associated with a novel transthyretin mis-sense mutation at codon 18 (TTRD 18G)
|
8579098 |
1996 |