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rs4765905

From SNPedia

Orientationplus
Stabilizedplus
Make rs4765905(C;C)
Make rs4765905(C;G)
Make rs4765905(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position2240418
GeneCACNA1C
is asnp
is mentioned by
dbSNPrs4765905
ebirs4765905
HLIrs4765905
Exacrs4765905
Varsomers4765905
Maprs4765905
PheGenIrs4765905
hapmaprs4765905
1000 genomesrs4765905
hgdprs4765905
ensemblrs4765905
gopubmedrs4765905
geneviewrs4765905
scholarrs4765905
googlers4765905
pharmgkbrs4765905
gwascentralrs4765905
openSNPrs4765905
23andMers4765905
23andMe allrs4765905
SNP Nexus

SNPshotrs4765905
SNPdbers4765905
MSV3drs4765905
GWAS Ctlgrs4765905
GMAF0.3035
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 21926974OA-icon.png]
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 22688191OA-icon.png]
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 26204268OA-icon.png] 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.