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rs10894294

From SNPedia

Orientationplus
Stabilizedplus
Make rs10894294(A;A)
Make rs10894294(A;C)
Make rs10894294(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position130960853
is asnp
is mentioned by
dbSNPrs10894294
ebirs10894294
HLIrs10894294
Exacrs10894294
Varsomers10894294
Maprs10894294
PheGenIrs10894294
hapmaprs10894294
1000 genomesrs10894294
hgdprs10894294
ensemblrs10894294
gopubmedrs10894294
geneviewrs10894294
scholarrs10894294
googlers10894294
pharmgkbrs10894294
gwascentralrs10894294
openSNPrs10894294
23andMers10894294
23andMe allrs10894294
SNP Nexus

SNPshotrs10894294
SNPdbers10894294
MSV3drs10894294
GWAS Ctlgrs10894294
GMAF0.4298
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
P-val 0.000003
Odds Ratio 1.0800 [1.05-1.12]
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 3E-7
Odds Ratio 1.1000 None