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rs10503253

From SNPedia

Orientationplus
Stabilizedplus
Make rs10503253(A;A)
Make rs10503253(A;C)
Make rs10503253(C;C)
ReferenceGRCh38 38.1/141
Chromosome8
Position4323322
GeneCSMD1
is asnp
is mentioned by
dbSNPrs10503253
ebirs10503253
HLIrs10503253
Exacrs10503253
Varsomers10503253
Maprs10503253
PheGenIrs10503253
hapmaprs10503253
1000 genomesrs10503253
hgdprs10503253
ensemblrs10503253
gopubmedrs10503253
geneviewrs10503253
scholarrs10503253
googlers10503253
pharmgkbrs10503253
gwascentralrs10503253
openSNPrs10503253
23andMers10503253
23andMe allrs10503253
SNP Nexus

SNPshotrs10503253
SNPdbers10503253
MSV3drs10503253
GWAS Ctlgrs10503253
GMAF0.1942
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 21926974OA-icon.png]
Trait
Title Genome-wide association study identifies five new schizophrenia loci.
Risk Allele A
P-val 2E-8
Odds Ratio 1.1600 [1.11-1.21]
GWAS snp
PMID [PMID 23453885OA-icon.png]
Trait Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)
Title Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
Risk Allele
P-val 4E-8
Odds Ratio NR NR


[PMID 23839771] Neural effects of the CSMD1 genome-wide associated schizophrenia risk variant rs10503253


[PMID 23320435] Neuropsychological effects of the CSMD1 genome-wide associated schizophrenia risk variant rs10503253.


[PMID 27377754] No association between the rs10503253 polymorphism in the CSMD1 gene and schizophrenia in a Han Chinese population.