rs3733591
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs3733591(A;A) |
| Make rs3733591(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 9920506 |
| Gene | SLC2A9 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3733591 |
| dbSNP (classic) | rs3733591 |
| ClinGen | rs3733591 |
| ebi | rs3733591 |
| HLI | rs3733591 |
| Exac | rs3733591 |
| Gnomad | rs3733591 |
| Varsome | rs3733591 |
| LitVar | rs3733591 |
| Map | rs3733591 |
| PheGenI | rs3733591 |
| Biobank | rs3733591 |
| 1000 genomes | rs3733591 |
| hgdp | rs3733591 |
| ensembl | rs3733591 |
| geneview | rs3733591 |
| scholar | rs3733591 |
| rs3733591 | |
| pharmgkb | rs3733591 |
| gwascentral | rs3733591 |
| openSNP | rs3733591 |
| 23andMe | rs3733591 |
| SNPshot | rs3733591 |
| SNPdbe | rs3733591 |
| MSV3d | rs3733591 |
| GWAS Ctlg | rs3733591 |
| GMAF | 0.2938 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19723617] Associations of a nonsynonymous variant in SLC2A9 with gouty arthritis and uric acid levels in Han Chinese and Solomon Islanders
[PMID 21658257
] The SLC2A9 non-synonymous Arg265His variant and gout; evidence for a population-specific effect on severity
[PMID 18759275] Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish.
[PMID 25867401] Polymorphisms of uric transporter proteins in the pathogenesis of gout in a Chinese Han population
[PMID 27511497] Association analysis of five SNP variants with gout in the Minnan population in China.
| ClinVar | |
|---|---|
| Risk | rs3733591(A;A) |
| Alt | rs3733591(A;A) |
| Reference | Rs3733591(G;G) |
| Significance | Non-pathogenic |
| Disease | Familial renal hypouricemia |
| Variation | info |
| Gene | SLC2A9 |
| CLNDBN | Familial renal hypouricemia |
| Reversed | 1 |
| HGVS | NC_000004.11:g.9922130C>T |
| CLNSRC | |
| CLNACC | RCV000317105.1, |
[PMID 30350810] Association of solute carrier family 2, member 9 (SLC2A9) genetic variant rs3733591 with gout in a Malay sample set.
[PMID 32183743] ABCG2 rs2231142 variant in hyperuricemia is modified by SLC2A9 and SLC22A12 polymorphisms and cardiovascular risk factors in an elderly community-dwelling population.
