rs11231825
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs11231825(C;C) |
Make rs11231825(C;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 11 |
Position | 64592802 |
Gene | SLC22A12 |
is a | snp |
is | mentioned by |
dbSNP | rs11231825 |
dbSNP (classic) | rs11231825 |
ClinGen | rs11231825 |
ebi | rs11231825 |
HLI | rs11231825 |
Exac | rs11231825 |
Gnomad | rs11231825 |
Varsome | rs11231825 |
LitVar | rs11231825 |
Map | rs11231825 |
PheGenI | rs11231825 |
Biobank | rs11231825 |
1000 genomes | rs11231825 |
hgdp | rs11231825 |
ensembl | rs11231825 |
geneview | rs11231825 |
scholar | rs11231825 |
rs11231825 | |
pharmgkb | rs11231825 |
gwascentral | rs11231825 |
openSNP | rs11231825 |
23andMe | rs11231825 |
SNPshot | rs11231825 |
SNPdbe | rs11231825 |
MSV3d | rs11231825 |
GWAS Ctlg | rs11231825 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 25128519] Tubular urate transporter gene polymorphisms differentiate patients with gout who have normal and decreased urinary uric acid excretion
ClinVar | |
---|---|
Risk | rs11231825(C;C) |
Alt | rs11231825(C;C) |
Reference | Rs11231825(T;T) |
Significance | Non-pathogenic |
Disease | Familial renal hypouricemia |
Variation | info |
Gene | SLC22A12 |
CLNDBN | Familial renal hypouricemia |
Reversed | 0 |
HGVS | NC_000011.9:g.64360274T>C |
CLNSRC | |
CLNACC | RCV000286659.1, |