rs4765905

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
google	rs4765905
pharmgkb	rs4765905
gwascentral	rs4765905
openSNP	rs4765905
23andMe	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.