rs7727656
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7727656(G;G) |
| Make rs7727656(G;T) |
| Make rs7727656(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 25760570 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7727656 |
| dbSNP (classic) | rs7727656 |
| ClinGen | rs7727656 |
| ebi | rs7727656 |
| HLI | rs7727656 |
| Exac | rs7727656 |
| Gnomad | rs7727656 |
| Varsome | rs7727656 |
| LitVar | rs7727656 |
| Map | rs7727656 |
| PheGenI | rs7727656 |
| Biobank | rs7727656 |
| 1000 genomes | rs7727656 |
| hgdp | rs7727656 |
| ensembl | rs7727656 |
| geneview | rs7727656 |
| scholar | rs7727656 |
| rs7727656 | |
| pharmgkb | rs7727656 |
| gwascentral | rs7727656 |
| openSNP | rs7727656 |
| 23andMe | rs7727656 |
| SNPshot | rs7727656 |
| SNPdbe | rs7727656 |
| MSV3d | rs7727656 |
| GWAS Ctlg | rs7727656 |
| GMAF | 0.4206 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 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 | 0.000008 |
| Odds Ratio | NR NR |
