rs9621532
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs9621532(A;C) |
| Make rs9621532(C;C) |
| Reference | GRCh37 37.1/131 |
| Chromosome | 22 |
| Position | 32688525 |
| Gene | SYN3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9621532 |
| dbSNP (classic) | rs9621532 |
| ClinGen | rs9621532 |
| ebi | rs9621532 |
| HLI | rs9621532 |
| Exac | rs9621532 |
| Gnomad | rs9621532 |
| Varsome | rs9621532 |
| LitVar | rs9621532 |
| Map | rs9621532 |
| PheGenI | rs9621532 |
| Biobank | rs9621532 |
| 1000 genomes | rs9621532 |
| hgdp | rs9621532 |
| ensembl | rs9621532 |
| geneview | rs9621532 |
| scholar | rs9621532 |
| rs9621532 | |
| pharmgkb | rs9621532 |
| gwascentral | rs9621532 |
| openSNP | rs9621532 |
| 23andMe | rs9621532 |
| SNPshot | rs9621532 |
| SNPdbe | rs9621532 |
| MSV3d | rs9621532 |
| GWAS Ctlg | rs9621532 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 20385826
] Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC)
| GWAS snp | |
|---|---|
| PMID | [PMID 20385819]
|
| Trait | Age-related macular degeneration |
| Title | Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration |
| Risk Allele | A |
| P-val | 1E-11 |
| Odds Ratio | 1.41 [1.27-1.57] |
| GWAS snp | |
|---|---|
| PMID | [PMID 21665990]
|
| Trait | |
| Title | Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. |
| Risk Allele | |
| P-val | 2E-15 |
| Odds Ratio | 1.5900 [NR] |
[PMID 22171703] An rs9621532 variant near the TIMP3 gene is not associated with neovascular age-related macular degeneration and polypoidal choroidal vasculopathy in a Chinese Han population
[PMID 23422939] Influence of TIMP3/SYN3 polymorphisms on the phenotypic presentation of age-related macular degeneration.
[PMID 32330537] Associations of IL6 rs1800795, BLK rs13277113, TIMP3 rs9621532, IL1RL1 rs1041973 and IL1RAP rs4624606 single gene polymorphisms with laryngeal squamous cell carcinoma.
