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rs7914558

From SNPedia

Orientationplus
Stabilizedplus
Make rs7914558(A;A)
Make rs7914558(A;G)
Make rs7914558(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position103016151
GeneCNNM2
is asnp
is mentioned by
dbSNPrs7914558
ebirs7914558
HLIrs7914558
Exacrs7914558
Varsomers7914558
Maprs7914558
PheGenIrs7914558
hapmaprs7914558
1000 genomesrs7914558
hgdprs7914558
ensemblrs7914558
gopubmedrs7914558
geneviewrs7914558
scholarrs7914558
googlers7914558
pharmgkbrs7914558
gwascentralrs7914558
openSNPrs7914558
23andMers7914558
23andMe allrs7914558
SNP Nexus

SNPshotrs7914558
SNPdbers7914558
MSV3drs7914558
GWAS Ctlgrs7914558
GMAF0.4293
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21926974OA-icon.png]
Trait
Title Genome-wide association study identifies five new schizophrenia loci.
Risk Allele G
P-val 2E-8
Odds Ratio 1.2200 [1.15-1.29]


[PMID 22520855] Association study of a new schizophrenia susceptibility locus of 10q24.32-33 in a Han Chinese population.

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 2E-9
Odds Ratio NR NR


[PMID 24160291OA-icon.png] The impact of the genome-wide supported variant in the cyclin M2 gene on gray matter morphology in schizophrenia


[PMID 25833874] Influences of schizophrenia risk variant rs7914558 at CNNM2 on brain structure


[PMID 27481827] Testing the Validity of Taxonic Schizotypy Using Genetic and Environmental Risk Variables.