rs337847
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs337847(A;A) |
| Make rs337847(A;G) |
| Make rs337847(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 78964065 |
| Gene | ARSB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs337847 |
| dbSNP (classic) | rs337847 |
| ClinGen | rs337847 |
| ebi | rs337847 |
| HLI | rs337847 |
| Exac | rs337847 |
| Gnomad | rs337847 |
| Varsome | rs337847 |
| LitVar | rs337847 |
| Map | rs337847 |
| PheGenI | rs337847 |
| Biobank | rs337847 |
| 1000 genomes | rs337847 |
| hgdp | rs337847 |
| ensembl | rs337847 |
| geneview | rs337847 |
| scholar | rs337847 |
| rs337847 | |
| pharmgkb | rs337847 |
| gwascentral | rs337847 |
| openSNP | rs337847 |
| 23andMe | rs337847 |
| SNPshot | rs337847 |
| SNPdbe | rs337847 |
| MSV3d | rs337847 |
| GWAS Ctlg | rs337847 |
| GMAF | 0.1405 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 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 | 0.000007 |
| Odds Ratio | NR NR |
