rs10850408
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10850408(C;C) |
| Make rs10850408(C;T) |
| Make rs10850408(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 114942588 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10850408 |
| dbSNP (classic) | rs10850408 |
| ClinGen | rs10850408 |
| ebi | rs10850408 |
| HLI | rs10850408 |
| Exac | rs10850408 |
| Gnomad | rs10850408 |
| Varsome | rs10850408 |
| LitVar | rs10850408 |
| Map | rs10850408 |
| PheGenI | rs10850408 |
| Biobank | rs10850408 |
| 1000 genomes | rs10850408 |
| hgdp | rs10850408 |
| ensembl | rs10850408 |
| geneview | rs10850408 |
| scholar | rs10850408 |
| rs10850408 | |
| pharmgkb | rs10850408 |
| gwascentral | rs10850408 |
| openSNP | rs10850408 |
| 23andMe | rs10850408 |
| SNPshot | rs10850408 |
| SNPdbe | rs10850408 |
| MSV3d | rs10850408 |
| GWAS Ctlg | rs10850408 |
| GMAF | 0.2649 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22159054 ]
|
| Trait | |
| Title | A comprehensive genetic association study of Alzheimer disease in African Americans. |
| Risk Allele | |
| P-val | 9E-7 |
| Odds Ratio | 1.5900 None |
