rs13113918
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs13113918(A;G) |
| Make rs13113918(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 9996869 |
| Gene | LOC105374476, SLC2A9 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs13113918 |
| dbSNP (classic) | rs13113918 |
| ClinGen | rs13113918 |
| ebi | rs13113918 |
| HLI | rs13113918 |
| Exac | rs13113918 |
| Gnomad | rs13113918 |
| Varsome | rs13113918 |
| LitVar | rs13113918 |
| Map | rs13113918 |
| PheGenI | rs13113918 |
| Biobank | rs13113918 |
| 1000 genomes | rs13113918 |
| hgdp | rs13113918 |
| ensembl | rs13113918 |
| geneview | rs13113918 |
| scholar | rs13113918 |
| rs13113918 | |
| pharmgkb | rs13113918 |
| gwascentral | rs13113918 |
| openSNP | rs13113918 |
| 23andMe | rs13113918 |
| SNPshot | rs13113918 |
| SNPdbe | rs13113918 |
| MSV3d | rs13113918 |
| GWAS Ctlg | rs13113918 |
| GMAF | 0.1607 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 21186168
] Association between SLC2A9 transporter gene variants and uric acid phenotypes in African American and white families
[PMID 23272134] Changes in uric acid levels following bariatric surgery are not associated with SLC2A9 variants in the Swedish Obese Subjects Study
| ClinVar | |
|---|---|
| Risk | rs13113918(G;G) |
| Alt | rs13113918(G;G) |
| Reference | Rs13113918(A;A) |
| Significance | Non-pathogenic |
| Disease | Familial renal hypouricemia |
| Variation | info |
| Gene | SLC2A9 |
| CLNDBN | Familial renal hypouricemia |
| Reversed | 0 |
| HGVS | NC_000004.11:g.9998493A>G |
| CLNSRC | |
| CLNACC | RCV000320934.1, |
