rs927675
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs927675(G;G) |
| Make rs927675(G;T) |
| Make rs927675(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 28094004 |
| Gene | MPP7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs927675 |
| dbSNP (classic) | rs927675 |
| ClinGen | rs927675 |
| ebi | rs927675 |
| HLI | rs927675 |
| Exac | rs927675 |
| Gnomad | rs927675 |
| Varsome | rs927675 |
| LitVar | rs927675 |
| Map | rs927675 |
| PheGenI | rs927675 |
| Biobank | rs927675 |
| 1000 genomes | rs927675 |
| hgdp | rs927675 |
| ensembl | rs927675 |
| geneview | rs927675 |
| scholar | rs927675 |
| rs927675 | |
| pharmgkb | rs927675 |
| gwascentral | rs927675 |
| openSNP | rs927675 |
| 23andMe | rs927675 |
| SNPshot | rs927675 |
| SNPdbe | rs927675 |
| MSV3d | rs927675 |
| GWAS Ctlg | rs927675 |
| GMAF | 0.3329 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21116278 ]
|
| Trait | |
| Title | Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease |
| Risk Allele | |
| P-val | 0.000002 |
| Odds Ratio | 0.0002 [NR] unit increase (main effect) |
