rs2373000
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2373000(C;C) |
| Make rs2373000(C;T) |
| Make rs2373000(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 2 |
| Position | 37365485 |
| Gene | QPCT |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2373000 |
| dbSNP (classic) | rs2373000 |
| ClinGen | rs2373000 |
| ebi | rs2373000 |
| HLI | rs2373000 |
| Exac | rs2373000 |
| Gnomad | rs2373000 |
| Varsome | rs2373000 |
| LitVar | rs2373000 |
| Map | rs2373000 |
| PheGenI | rs2373000 |
| Biobank | rs2373000 |
| 1000 genomes | rs2373000 |
| hgdp | rs2373000 |
| ensembl | rs2373000 |
| geneview | rs2373000 |
| scholar | rs2373000 |
| rs2373000 | |
| pharmgkb | rs2373000 |
| gwascentral | rs2373000 |
| openSNP | rs2373000 |
| 23andMe | rs2373000 |
| SNPshot | rs2373000 |
| SNPdbe | rs2373000 |
| MSV3d | rs2373000 |
| GWAS Ctlg | rs2373000 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23974872 |
| Trait | Schizophrenia |
| Title | Genome-wide association analysis identifies 13 new risk loci for schizophrenia. |
| Risk Allele | T |
| P-val | 7E-9 |
| Odds Ratio | 1.09 [1.06-1.11] |
[PMID 26492838] Common variants in QPCT gene confer risk of schizophrenia in the Han Chinese population
[PMID 26572640] Common Polymorphisms Within QPCT Gene Are Associated with the Susceptibility of Schizophrenia in a Han Chinese Population
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 2
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
