rs6449213
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 2 | ~4x higher risk for hyperuracemia |
| (C;T) | ~2x higher risk for hyperuracemia | |
| (T;T) | 0 | normal |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 9992591 |
| Gene | LOC105374476, SLC2A9 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6449213 |
| dbSNP (classic) | rs6449213 |
| ClinGen | rs6449213 |
| ebi | rs6449213 |
| HLI | rs6449213 |
| Exac | rs6449213 |
| Gnomad | rs6449213 |
| Varsome | rs6449213 |
| LitVar | rs6449213 |
| Map | rs6449213 |
| PheGenI | rs6449213 |
| Biobank | rs6449213 |
| 1000 genomes | rs6449213 |
| hgdp | rs6449213 |
| ensembl | rs6449213 |
| geneview | rs6449213 |
| scholar | rs6449213 |
| rs6449213 | |
| pharmgkb | rs6449213 |
| gwascentral | rs6449213 |
| openSNP | rs6449213 |
| 23andMe | rs6449213 |
| SNPshot | rs6449213 |
| SNPdbe | rs6449213 |
| MSV3d | rs6449213 |
| GWAS Ctlg | rs6449213 |
| GMAF | 0.1299 |
| Max Magnitude | 2 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
This is basically a surrogate for rs7442295, and thus associated with higher serum urate levels.
| OMIM | 606142 |
| Desc | SOLUTE CARRIER FAMILY 2 (FACILITATED GLUCOSE TRANSPORTER), MEMBER |
| Variant | |
| Related | also |
[PMID 20589538] Variation in the Uric Acid Transporter Gene SLC2A9 and Its Association with AAO of Parkinson's Disease
[PMID 18179892
] Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia.
[PMID 18398472
] Association of common polymorphisms in GLUT9 gene with gout but not with coronary artery disease in a large case-control study.
[PMID 18487473
] Sex-specific association of the putative fructose transporter SLC2A9 variants with uric acid levels is modified by BMI.
[PMID 18606621
] SLC2A9--a fructose transporter identified as a novel uric acid transporter.
[PMID 18834626
] Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study.
[PMID 19260141
] Genome-wide association study of biochemical traits in Korcula Island, Croatia.
[PMID 20053405
] Sex and age interaction with genetic association of atherogenic uric acid concentrations.
[PMID 20162742
] Predictive value of 8 genetic loci for serum uric acid concentration.
[PMID 20162743
] Common variants in SLC17A3 gene affect intra-personal variation in serum uric acid levels in longitudinal time series.
[PMID 20162744
] Interactions between genetic variants in glucose transporter type 9 (SLC2A9) and dietary habits in serum uric acid regulation.
[PMID 20162745
] Association of nephrolithiasis and gene for glucose transporter type 9 (SLC2A9): study of 145 patients.
[PMID 20348110
] Bayesian methods for instrumental variable analysis with genetic instruments ('Mendelian randomization'): example with urate transporter SLC2A9 as an instrumental variable for effect of urate levels on metabolic syndrome.
[PMID 21294900
] A genome-wide association study of serum uric acid in African Americans.
| GWAS snp | |
|---|---|
| PMID | [PMID 23703922 |
| Trait | Uric acid levels |
| Title | A genome wide association study of plasma uric acid levels in obese cases and never-overweight controls. |
| Risk Allele | |
| P-val | 3E-12 |
| Odds Ratio | NR NR |
[PMID 26552468
] Genetic analysis of ABCG2 and SLC2A9 gene polymorphisms in gouty arthritis in a Korean population
| ClinVar | |
|---|---|
| Risk | Rs6449213(T;T) |
| Alt | Rs6449213(T;T) |
| Reference | Rs6449213(C;C) |
| Significance | Other |
| Disease | Uric acid concentration |
| Variation | info |
| Gene | SLC2A9 |
| CLNDBN | Uric acid concentration, serum, quantitative trait locus 2 |
| Reversed | 0 |
| HGVS | NC_000004.11:g.9994215C>T |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000004857.2, |
- Is a snp
- In dbSNP
- SNPs on chromosome 4
- Has genotype
- Has population
- Uses omim
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Affy500k
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
