rs17693963
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 |
| Make rs17693963(A;C) |
| Make rs17693963(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 27742386 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17693963 |
| dbSNP (classic) | rs17693963 |
| ClinGen | rs17693963 |
| ebi | rs17693963 |
| HLI | rs17693963 |
| Exac | rs17693963 |
| Gnomad | rs17693963 |
| Varsome | rs17693963 |
| LitVar | rs17693963 |
| Map | rs17693963 |
| PheGenI | rs17693963 |
| Biobank | rs17693963 |
| 1000 genomes | rs17693963 |
| hgdp | rs17693963 |
| ensembl | rs17693963 |
| geneview | rs17693963 |
| scholar | rs17693963 |
| rs17693963 | |
| pharmgkb | rs17693963 |
| gwascentral | rs17693963 |
| openSNP | rs17693963 |
| 23andMe | rs17693963 |
| SNPshot | rs17693963 |
| SNPdbe | rs17693963 |
| MSV3d | rs17693963 |
| GWAS Ctlg | rs17693963 |
| GMAF | 0.04729 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22688191 ]
|
| Trait | |
| Title | Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder. |
| Risk Allele | |
| P-val | 3E-11 |
| Odds Ratio | 1.2400 None |
[PMID 19571809] Common variants on chromosome 6p22.1 are associated with schizophrenia.
| GWAS snp | |
|---|---|
| PMID | [PMID 24166486]
|
| Trait | Schizophrenia, schizoaffective disorder or bipolar disorder |
| Title | GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus. |
| Risk Allele | |
| P-val | 2E-9 |
| Odds Ratio | NR NR |
| GWAS snp | |
|---|---|
| PMID | [PMID 24280982]
|
| Trait | Schizophrenia or bipolar disorder |
| Title | Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia. |
| Risk Allele | |
| P-val | 3E-11 |
| Odds Ratio | NR NR |
