rs9862
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs9862(C;C) |
| Make rs9862(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 32857293 |
| Gene | SYN3, TIMP3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9862 |
| dbSNP (classic) | rs9862 |
| ClinGen | rs9862 |
| ebi | rs9862 |
| HLI | rs9862 |
| Exac | rs9862 |
| Gnomad | rs9862 |
| Varsome | rs9862 |
| LitVar | rs9862 |
| Map | rs9862 |
| PheGenI | rs9862 |
| Biobank | rs9862 |
| 1000 genomes | rs9862 |
| hgdp | rs9862 |
| ensembl | rs9862 |
| geneview | rs9862 |
| scholar | rs9862 |
| rs9862 | |
| pharmgkb | rs9862 |
| gwascentral | rs9862 |
| openSNP | rs9862 |
| 23andMe | rs9862 |
| SNPshot | rs9862 |
| SNPdbe | rs9862 |
| MSV3d | rs9862 |
| GWAS Ctlg | rs9862 |
| GMAF | 0.3581 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19766700
] Association and expression study of synapsin III and schizophrenia
[PMID 18716610] Genomic screening identifies novel linkages and provides further evidence for a role of MYH9 in nonsyndromic cleft lip and palate.
[PMID 23527119] Genetic polymorphisms at TIMP3 are associated with survival of adenocarcinoma of the gastroesophageal junction
[PMID 26579821] Polymorphisms and Plasma Levels of Tissue Inhibitor of Metalloproteinase-3: Impact on Genetic Susceptibility and Clinical Outcome of Oral Cancer
| ClinVar | |
|---|---|
| Risk | rs9862(C;C) |
| Alt | rs9862(C;C) |
| Reference | Rs9862(T;T) |
| Significance | Non-pathogenic |
| Disease | not specified Pseudoinflammatory fundus dystrophy |
| Variation | info |
| Gene | SYN3 TIMP3 |
| CLNDBN | not specified Pseudoinflammatory fundus dystrophy |
| Reversed | 0 |
| HGVS | NC_000022.10:g.33253280T>C |
| CLNSRC | |
| CLNACC | RCV000254229.1, RCV000384049.1, |
