rs13037749
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs13037749(A;A) |
| Make rs13037749(A;G) |
| Make rs13037749(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 41435919 |
| Gene | CHD6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs13037749 |
| dbSNP (classic) | rs13037749 |
| ClinGen | rs13037749 |
| ebi | rs13037749 |
| HLI | rs13037749 |
| Exac | rs13037749 |
| Gnomad | rs13037749 |
| Varsome | rs13037749 |
| LitVar | rs13037749 |
| Map | rs13037749 |
| PheGenI | rs13037749 |
| Biobank | rs13037749 |
| 1000 genomes | rs13037749 |
| hgdp | rs13037749 |
| ensembl | rs13037749 |
| geneview | rs13037749 |
| scholar | rs13037749 |
| rs13037749 | |
| pharmgkb | rs13037749 |
| gwascentral | rs13037749 |
| openSNP | rs13037749 |
| 23andMe | rs13037749 |
| SNPshot | rs13037749 |
| SNPdbe | rs13037749 |
| MSV3d | rs13037749 |
| GWAS Ctlg | rs13037749 |
| GMAF | 0.02893 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22745009 ]
|
| Trait | |
| Title | Multiple loci influencing hippocampal degeneration identified by genome scan. |
| Risk Allele | A |
| P-val | 0.000008 |
| Odds Ratio | None None |
