rs10503256
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10503256(A;A) |
| Make rs10503256(A;G) |
| Make rs10503256(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 4356657 |
| Gene | CSMD1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10503256 |
| dbSNP (classic) | rs10503256 |
| ClinGen | rs10503256 |
| ebi | rs10503256 |
| HLI | rs10503256 |
| Exac | rs10503256 |
| Gnomad | rs10503256 |
| Varsome | rs10503256 |
| LitVar | rs10503256 |
| Map | rs10503256 |
| PheGenI | rs10503256 |
| Biobank | rs10503256 |
| 1000 genomes | rs10503256 |
| hgdp | rs10503256 |
| ensembl | rs10503256 |
| geneview | rs10503256 |
| scholar | rs10503256 |
| rs10503256 | |
| pharmgkb | rs10503256 |
| gwascentral | rs10503256 |
| openSNP | rs10503256 |
| 23andMe | rs10503256 |
| SNPshot | rs10503256 |
| SNPdbe | rs10503256 |
| MSV3d | rs10503256 |
| GWAS Ctlg | rs10503256 |
| GMAF | 0.4178 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 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 | 9E-7 |
| Odds Ratio | 1.1000 None |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 8
- 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
