rs4789932
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs4789932(C;C) |
| Make rs4789932(C;T) |
| Make rs4789932(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 78928193 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4789932 |
| dbSNP (classic) | rs4789932 |
| ClinGen | rs4789932 |
| ebi | rs4789932 |
| HLI | rs4789932 |
| Exac | rs4789932 |
| Gnomad | rs4789932 |
| Varsome | rs4789932 |
| LitVar | rs4789932 |
| Map | rs4789932 |
| PheGenI | rs4789932 |
| Biobank | rs4789932 |
| 1000 genomes | rs4789932 |
| hgdp | rs4789932 |
| ensembl | rs4789932 |
| geneview | rs4789932 |
| scholar | rs4789932 |
| rs4789932 | |
| pharmgkb | rs4789932 |
| gwascentral | rs4789932 |
| openSNP | rs4789932 |
| 23andMe | rs4789932 |
| SNPshot | rs4789932 |
| SNPdbe | rs4789932 |
| MSV3d | rs4789932 |
| GWAS Ctlg | rs4789932 |
| GMAF | 0.4711 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
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| ||
[PMID 23491141] Polymorphic variation within the ADAMTS2, ADAMTS14, ADAMTS5, ADAM12 and TIMP2 genes and the risk of Achilles tendon pathology: A genetic association study
[PMID 19431211
] Polymorphisms in tissue inhibitors of metalloproteinases-2 and -3 and breast cancer susceptibility and survival.
[PMID 30755371] Are MMP3, MMP8 and TIMP2 gene variants associated with anterior cruciate ligament rupture susceptibility?
[PMID 31772230] Relationship of common variants in MPP7, TIMP2 and CASP8 genes with the risk of chronic achilles tendinopathy.
