rs6782299
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6782299(G;G) |
| Make rs6782299(G;T) |
| Make rs6782299(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 180832914 |
| Gene | LOC101928882 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6782299 |
| dbSNP (classic) | rs6782299 |
| ClinGen | rs6782299 |
| ebi | rs6782299 |
| HLI | rs6782299 |
| Exac | rs6782299 |
| Gnomad | rs6782299 |
| Varsome | rs6782299 |
| LitVar | rs6782299 |
| Map | rs6782299 |
| PheGenI | rs6782299 |
| Biobank | rs6782299 |
| 1000 genomes | rs6782299 |
| hgdp | rs6782299 |
| ensembl | rs6782299 |
| geneview | rs6782299 |
| scholar | rs6782299 |
| rs6782299 | |
| pharmgkb | rs6782299 |
| gwascentral | rs6782299 |
| openSNP | rs6782299 |
| 23andMe | rs6782299 |
| SNPshot | rs6782299 |
| SNPdbe | rs6782299 |
| MSV3d | rs6782299 |
| GWAS Ctlg | rs6782299 |
| GMAF | 0.1529 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19571811 ]
|
| Trait | Schizophrenia |
| Title | Common polygenic variation contributes to risk of schizophrenia and bipolar disorder |
| Risk Allele | T |
| P-val | 1E-7 |
| Odds Ratio | 1.10 None |
[PMID 21359210] Pooled genome-wide analysis to identify novel risk loci for pediatric allergic asthma.
