rs10207628
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10207628(C;C) |
| Make rs10207628(C;G) |
| Make rs10207628(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 127094445 |
| Gene | BIN1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10207628 |
| dbSNP (classic) | rs10207628 |
| ClinGen | rs10207628 |
| ebi | rs10207628 |
| HLI | rs10207628 |
| Exac | rs10207628 |
| Gnomad | rs10207628 |
| Varsome | rs10207628 |
| LitVar | rs10207628 |
| Map | rs10207628 |
| PheGenI | rs10207628 |
| Biobank | rs10207628 |
| 1000 genomes | rs10207628 |
| hgdp | rs10207628 |
| ensembl | rs10207628 |
| geneview | rs10207628 |
| scholar | rs10207628 |
| rs10207628 | |
| pharmgkb | rs10207628 |
| gwascentral | rs10207628 |
| openSNP | rs10207628 |
| 23andMe | rs10207628 |
| SNPshot | rs10207628 |
| SNPdbe | rs10207628 |
| MSV3d | rs10207628 |
| GWAS Ctlg | rs10207628 |
| GMAF | 0.1818 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22005930 |
| Trait | |
| Title | Genome-wide association study of Alzheimer's disease with psychotic symptoms. |
| Risk Allele | |
| P-val | 0.000001 |
| Odds Ratio | 1.4100 None |
