rs723744
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs723744(A;A) |
Make rs723744(A;C) |
Make rs723744(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 31592513 |
Gene | TTR |
is a | snp |
is | mentioned by |
dbSNP | rs723744 |
dbSNP (classic) | rs723744 |
ClinGen | rs723744 |
ebi | rs723744 |
HLI | rs723744 |
Exac | rs723744 |
Gnomad | rs723744 |
Varsome | rs723744 |
LitVar | rs723744 |
Map | rs723744 |
PheGenI | rs723744 |
Biobank | rs723744 |
1000 genomes | rs723744 |
hgdp | rs723744 |
ensembl | rs723744 |
geneview | rs723744 |
scholar | rs723744 |
rs723744 | |
pharmgkb | rs723744 |
gwascentral | rs723744 |
openSNP | rs723744 |
23andMe | rs723744 |
SNPshot | rs723744 |
SNPdbe | rs723744 |
MSV3d | rs723744 |
GWAS Ctlg | rs723744 |
GMAF | 0.3632 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 22027013] Genetic analysis of genes involved in amyloid-β degradation and clearance in Alzheimer's disease
[PMID 16362527] An association study between the transthyretin (TTR) gene and mental retardation.
[PMID 19328595] Association of TTR polymorphisms with hippocampal atrophy in Alzheimer disease families.