rs4861387
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4861387(A;A) |
| Make rs4861387(A;G) |
| Make rs4861387(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 41266448 |
| Gene | UCHL1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4861387 |
| dbSNP (classic) | rs4861387 |
| ClinGen | rs4861387 |
| ebi | rs4861387 |
| HLI | rs4861387 |
| Exac | rs4861387 |
| Gnomad | rs4861387 |
| Varsome | rs4861387 |
| LitVar | rs4861387 |
| Map | rs4861387 |
| PheGenI | rs4861387 |
| Biobank | rs4861387 |
| 1000 genomes | rs4861387 |
| hgdp | rs4861387 |
| ensembl | rs4861387 |
| geneview | rs4861387 |
| scholar | rs4861387 |
| rs4861387 | |
| pharmgkb | rs4861387 |
| gwascentral | rs4861387 |
| openSNP | rs4861387 |
| 23andMe | rs4861387 |
| SNPshot | rs4861387 |
| SNPdbe | rs4861387 |
| MSV3d | rs4861387 |
| GWAS Ctlg | rs4861387 |
| GMAF | 0.1993 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 22688354] Lack of Genetic Association of the UCHL1 Gene with Alzheimer's Disease and Parkinson's Disease with Dementia
