rs38857
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs38857(C;C) |
| Make rs38857(C;T) |
| Make rs38857(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 116725359 |
| Gene | MET |
| is a | snp |
| is | mentioned by |
| dbSNP | rs38857 |
| dbSNP (classic) | rs38857 |
| ClinGen | rs38857 |
| ebi | rs38857 |
| HLI | rs38857 |
| Exac | rs38857 |
| Gnomad | rs38857 |
| Varsome | rs38857 |
| LitVar | rs38857 |
| Map | rs38857 |
| PheGenI | rs38857 |
| Biobank | rs38857 |
| 1000 genomes | rs38857 |
| hgdp | rs38857 |
| ensembl | rs38857 |
| geneview | rs38857 |
| scholar | rs38857 |
| rs38857 | |
| pharmgkb | rs38857 |
| gwascentral | rs38857 |
| openSNP | rs38857 |
| 23andMe | rs38857 |
| SNPshot | rs38857 |
| SNPdbe | rs38857 |
| MSV3d | rs38857 |
| GWAS Ctlg | rs38857 |
| GMAF | 0.2332 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20416453] c-MET pathway involvement in chronic rhinosinusitis: a genetic association analysis
[PMID 19002214
] MET and autism susceptibility: family and case-control studies.
[PMID 20011629] The hepatocyte growth factor receptor (MET) gene is not associated with refractive error and ocular biometrics in a Caucasian population.
[PMID 20080979] Association of genetic variation in the MET proto-oncogene with schizophrenia and general cognitive ability.
[PMID 24766640] Evaluation of MYOC, ACAN, HGF, and MET as Candidate Genes for High Myopia in a Han Chinese Population
