rs4667682
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4667682(C;C) |
| Make rs4667682(C;T) |
| Make rs4667682(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 171271410 |
| Gene | LOC105373737 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4667682 |
| dbSNP (classic) | rs4667682 |
| ClinGen | rs4667682 |
| ebi | rs4667682 |
| HLI | rs4667682 |
| Exac | rs4667682 |
| Gnomad | rs4667682 |
| Varsome | rs4667682 |
| LitVar | rs4667682 |
| Map | rs4667682 |
| PheGenI | rs4667682 |
| Biobank | rs4667682 |
| 1000 genomes | rs4667682 |
| hgdp | rs4667682 |
| ensembl | rs4667682 |
| geneview | rs4667682 |
| scholar | rs4667682 |
| rs4667682 | |
| pharmgkb | rs4667682 |
| gwascentral | rs4667682 |
| openSNP | rs4667682 |
| 23andMe | rs4667682 |
| SNPshot | rs4667682 |
| SNPdbe | rs4667682 |
| MSV3d | rs4667682 |
| GWAS Ctlg | rs4667682 |
| GMAF | 0.225 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22745009 ]
|
| Trait | |
| Title | Multiple loci influencing hippocampal degeneration identified by genome scan. |
| Risk Allele | C |
| P-val | 0.000005 |
| Odds Ratio | None None |
