rs4765905
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4765905(C;C) |
| Make rs4765905(C;G) |
| Make rs4765905(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 2240418 |
| Gene | CACNA1C |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4765905 |
| dbSNP (classic) | rs4765905 |
| ClinGen | rs4765905 |
| ebi | rs4765905 |
| HLI | rs4765905 |
| Exac | rs4765905 |
| Gnomad | rs4765905 |
| Varsome | rs4765905 |
| LitVar | rs4765905 |
| Map | rs4765905 |
| PheGenI | rs4765905 |
| Biobank | rs4765905 |
| 1000 genomes | rs4765905 |
| hgdp | rs4765905 |
| ensembl | rs4765905 |
| geneview | rs4765905 |
| scholar | rs4765905 |
| rs4765905 | |
| pharmgkb | rs4765905 |
| gwascentral | rs4765905 |
| openSNP | rs4765905 |
| 23andMe | rs4765905 |
| 23andMe all | rs4765905 |
| SNPshot | rs4765905 |
| SNPdbe | rs4765905 |
| MSV3d | rs4765905 |
| GWAS Ctlg | rs4765905 |
| GMAF | 0.3035 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21926974 ]
|
| Trait | |
| Title | Genome-wide association study identifies five new schizophrenia loci. |
| Risk Allele | |
| P-val | 0.000002 |
| Odds Ratio | 1.0800 [1.05-1.11] |
| 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 | 2E-7 |
| Odds Ratio | 1.1100 None |
[PMID 26204268] Schizophrenia Related Variants in CACNA1C also Confer Risk of Autism
[PMID 26276307] Meta-analysis of data from the Psychiatric Genomics Consortium and additional samples supports association of CACNA1C with risk for schizophrenia
[PMID 27276213] Functional Characterization of Schizophrenia-Associated Variation in CACNA1C.
