rs12261764
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12261764(G;G) |
| Make rs12261764(G;T) |
| Make rs12261764(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 120762869 |
| Gene | LOC105378516, WDR11-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12261764 |
| dbSNP (classic) | rs12261764 |
| ClinGen | rs12261764 |
| ebi | rs12261764 |
| HLI | rs12261764 |
| Exac | rs12261764 |
| Gnomad | rs12261764 |
| Varsome | rs12261764 |
| LitVar | rs12261764 |
| Map | rs12261764 |
| PheGenI | rs12261764 |
| Biobank | rs12261764 |
| 1000 genomes | rs12261764 |
| hgdp | rs12261764 |
| ensembl | rs12261764 |
| geneview | rs12261764 |
| scholar | rs12261764 |
| rs12261764 | |
| pharmgkb | rs12261764 |
| gwascentral | rs12261764 |
| openSNP | rs12261764 |
| 23andMe | rs12261764 |
| SNPshot | rs12261764 |
| SNPdbe | rs12261764 |
| MSV3d | rs12261764 |
| GWAS Ctlg | rs12261764 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 25140149
] Genetic variation modifies risk for neurodegeneration based on biomarker status
