rs38850
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs38850(A;A) |
| Make rs38850(A;G) |
| Make rs38850(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 116697595 |
| Gene | MET |
| is a | snp |
| is | mentioned by |
| dbSNP | rs38850 |
| dbSNP (classic) | rs38850 |
| ClinGen | rs38850 |
| ebi | rs38850 |
| HLI | rs38850 |
| Exac | rs38850 |
| Gnomad | rs38850 |
| Varsome | rs38850 |
| LitVar | rs38850 |
| Map | rs38850 |
| PheGenI | rs38850 |
| Biobank | rs38850 |
| 1000 genomes | rs38850 |
| hgdp | rs38850 |
| ensembl | rs38850 |
| geneview | rs38850 |
| scholar | rs38850 |
| rs38850 | |
| pharmgkb | rs38850 |
| gwascentral | rs38850 |
| openSNP | rs38850 |
| 23andMe | rs38850 |
| SNPshot | rs38850 |
| SNPdbe | rs38850 |
| MSV3d | rs38850 |
| GWAS Ctlg | rs38850 |
| GMAF | 0.1437 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 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 20401335] Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.
