rs11541790
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 5.5 | TTR-related amyloidosis |
(G;G) | 0 | common in clinvar |
Make rs11541790(A;A) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 18 |
Position | 31592956 |
Gene | TTR |
is a | snp |
is | mentioned by |
dbSNP | rs11541790 |
dbSNP (classic) | rs11541790 |
ClinGen | rs11541790 |
ebi | rs11541790 |
HLI | rs11541790 |
Exac | rs11541790 |
Gnomad | rs11541790 |
Varsome | rs11541790 |
LitVar | rs11541790 |
Map | rs11541790 |
PheGenI | rs11541790 |
Biobank | rs11541790 |
1000 genomes | rs11541790 |
hgdp | rs11541790 |
ensembl | rs11541790 |
geneview | rs11541790 |
scholar | rs11541790 |
rs11541790 | |
pharmgkb | rs11541790 |
gwascentral | rs11541790 |
openSNP | rs11541790 |
23andMe | rs11541790 |
SNPshot | rs11541790 |
SNPdbe | rs11541790 |
MSV3d | rs11541790 |
GWAS Ctlg | rs11541790 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
ClinVar | |
---|---|
Risk | rs11541790(A;A) |
Alt | rs11541790(A;A) |
Reference | Rs11541790(G;G) |
Significance | Other |
Disease | not provided |
Variation | info |
Gene | TTR |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000018.9:g.29172919C>T |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000159421.2, |