rs10243024
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10243024(A;A) |
| Make rs10243024(A;G) |
| Make rs10243024(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 116706549 |
| Gene | MET |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10243024 |
| dbSNP (classic) | rs10243024 |
| ClinGen | rs10243024 |
| ebi | rs10243024 |
| HLI | rs10243024 |
| Exac | rs10243024 |
| Gnomad | rs10243024 |
| Varsome | rs10243024 |
| LitVar | rs10243024 |
| Map | rs10243024 |
| PheGenI | rs10243024 |
| Biobank | rs10243024 |
| 1000 genomes | rs10243024 |
| hgdp | rs10243024 |
| ensembl | rs10243024 |
| geneview | rs10243024 |
| scholar | rs10243024 |
| rs10243024 | |
| pharmgkb | rs10243024 |
| gwascentral | rs10243024 |
| openSNP | rs10243024 |
| 23andMe | rs10243024 |
| SNPshot | rs10243024 |
| SNPdbe | rs10243024 |
| MSV3d | rs10243024 |
| GWAS Ctlg | rs10243024 |
| GMAF | 0.3177 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19010793 ]
|
| Trait | Multiple sclerosis (severity) |
| Title | Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis |
| Risk Allele | |
| P-val | 0.000006 |
| Odds Ratio | NR NR |
[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.
