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.