rs7192086
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7192086(A;A) |
| Make rs7192086(A;T) |
| Make rs7192086(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 12967754 |
| Gene | SHISA9 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7192086 |
| dbSNP (classic) | rs7192086 |
| ClinGen | rs7192086 |
| ebi | rs7192086 |
| HLI | rs7192086 |
| Exac | rs7192086 |
| Gnomad | rs7192086 |
| Varsome | rs7192086 |
| LitVar | rs7192086 |
| Map | rs7192086 |
| PheGenI | rs7192086 |
| Biobank | rs7192086 |
| 1000 genomes | rs7192086 |
| hgdp | rs7192086 |
| ensembl | rs7192086 |
| geneview | rs7192086 |
| scholar | rs7192086 |
| rs7192086 | |
| pharmgkb | rs7192086 |
| gwascentral | rs7192086 |
| openSNP | rs7192086 |
| 23andMe | rs7192086 |
| SNPshot | rs7192086 |
| SNPdbe | rs7192086 |
| MSV3d | rs7192086 |
| GWAS Ctlg | rs7192086 |
| GMAF | 0.2241 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS | |
|---|---|
| SNP | rs7192086 |
| PubMedID | [PMID 18677311] |
| Condition | Schizophrenia |
| Gene | Intergenic |
| Risk Allele | T |
| pValue | 6.00E-006 |
| OR | 1.12 |
| 95% CI | |
[PMID 19396477
] A novel 16p locus associated with BSCL2 hereditary motor neuronopathy: a genetic modifier?
[PMID 22005930] Genome-wide association study of Alzheimer's disease with psychotic symptoms.
