rs6881634
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6881634(A;A) |
| Make rs6881634(A;G) |
| Make rs6881634(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 78335030 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6881634 |
| dbSNP (classic) | rs6881634 |
| ClinGen | rs6881634 |
| ebi | rs6881634 |
| HLI | rs6881634 |
| Exac | rs6881634 |
| Gnomad | rs6881634 |
| Varsome | rs6881634 |
| LitVar | rs6881634 |
| Map | rs6881634 |
| PheGenI | rs6881634 |
| Biobank | rs6881634 |
| 1000 genomes | rs6881634 |
| hgdp | rs6881634 |
| ensembl | rs6881634 |
| geneview | rs6881634 |
| scholar | rs6881634 |
| rs6881634 | |
| pharmgkb | rs6881634 |
| gwascentral | rs6881634 |
| openSNP | rs6881634 |
| 23andMe | rs6881634 |
| SNPshot | rs6881634 |
| SNPdbe | rs6881634 |
| MSV3d | rs6881634 |
| GWAS Ctlg | rs6881634 |
| GMAF | 0.3705 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19668339 ]
|
| Trait | Hippocampal atrophy |
| Title | Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease |
| Risk Allele | |
| P-val | 0.000002 |
| Odds Ratio | NR NR |
