rs11723439
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11723439(C;C) |
Make rs11723439(C;T) |
Make rs11723439(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 9950195 |
Gene | SLC2A9 |
is a | snp |
is | mentioned by |
dbSNP | rs11723439 |
dbSNP (classic) | rs11723439 |
ClinGen | rs11723439 |
ebi | rs11723439 |
HLI | rs11723439 |
Exac | rs11723439 |
Gnomad | rs11723439 |
Varsome | rs11723439 |
LitVar | rs11723439 |
Map | rs11723439 |
PheGenI | rs11723439 |
Biobank | rs11723439 |
1000 genomes | rs11723439 |
hgdp | rs11723439 |
ensembl | rs11723439 |
geneview | rs11723439 |
scholar | rs11723439 |
rs11723439 | |
pharmgkb | rs11723439 |
gwascentral | rs11723439 |
openSNP | rs11723439 |
23andMe | rs11723439 |
SNPshot | rs11723439 |
SNPdbe | rs11723439 |
MSV3d | rs11723439 |
GWAS Ctlg | rs11723439 |
GMAF | 0.1212 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 21186168] Association between SLC2A9 transporter gene variants and uric acid phenotypes in African American and white families