rs4900442
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4900442(C;C) |
| Make rs4900442(C;T) |
| Make rs4900442(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 99691904 |
| Gene | CYP46A1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4900442 |
| dbSNP (classic) | rs4900442 |
| ClinGen | rs4900442 |
| ebi | rs4900442 |
| HLI | rs4900442 |
| Exac | rs4900442 |
| Gnomad | rs4900442 |
| Varsome | rs4900442 |
| LitVar | rs4900442 |
| Map | rs4900442 |
| PheGenI | rs4900442 |
| Biobank | rs4900442 |
| 1000 genomes | rs4900442 |
| hgdp | rs4900442 |
| ensembl | rs4900442 |
| geneview | rs4900442 |
| scholar | rs4900442 |
| rs4900442 | |
| pharmgkb | rs4900442 |
| gwascentral | rs4900442 |
| openSNP | rs4900442 |
| 23andMe | rs4900442 |
| SNPshot | rs4900442 |
| SNPdbe | rs4900442 |
| MSV3d | rs4900442 |
| GWAS Ctlg | rs4900442 |
| GMAF | 0.4431 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19286353] CYP46A1 variants influence Alzheimer's disease risk and brain cholesterol metabolism
[PMID 16960449] Intron 2 (T/C) CYP46 polymorphism is associated with Alzheimer's disease in Chinese patients.
