rs12638253
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12638253(C;C) |
| Make rs12638253(C;T) |
| Make rs12638253(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 156908302 |
| Gene | LEKR1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12638253 |
| dbSNP (classic) | rs12638253 |
| ClinGen | rs12638253 |
| ebi | rs12638253 |
| HLI | rs12638253 |
| Exac | rs12638253 |
| Gnomad | rs12638253 |
| Varsome | rs12638253 |
| LitVar | rs12638253 |
| Map | rs12638253 |
| PheGenI | rs12638253 |
| Biobank | rs12638253 |
| 1000 genomes | rs12638253 |
| hgdp | rs12638253 |
| ensembl | rs12638253 |
| geneview | rs12638253 |
| scholar | rs12638253 |
| rs12638253 | |
| pharmgkb | rs12638253 |
| gwascentral | rs12638253 |
| openSNP | rs12638253 |
| 23andMe | rs12638253 |
| SNPshot | rs12638253 |
| SNPdbe | rs12638253 |
| MSV3d | rs12638253 |
| GWAS Ctlg | rs12638253 |
| GMAF | 0.4963 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 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 | 0.000002 |
| Odds Ratio | NR NR |
[PMID 18985386] Genomewide association study for susceptibility genes contributing to familial Parkinson disease.
[PMID 19327735] Genome-wide linkage screen in familial Parkinson disease identifies loci on chromosomes 3 and 18.
