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rs12592967

From SNPedia

Orientationplus
Stabilizedplus
Make rs12592967(C;C)
Make rs12592967(C;T)
Make rs12592967(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position61578744
is asnp
is mentioned by
dbSNPrs12592967
ebirs12592967
HLIrs12592967
Exacrs12592967
Varsomers12592967
Maprs12592967
PheGenIrs12592967
hapmaprs12592967
1000 genomesrs12592967
hgdprs12592967
ensemblrs12592967
gopubmedrs12592967
geneviewrs12592967
scholarrs12592967
googlers12592967
pharmgkbrs12592967
gwascentralrs12592967
openSNPrs12592967
23andMers12592967
23andMe allrs12592967
SNP Nexus

SNPshotrs12592967
SNPdbers12592967
MSV3drs12592967
GWAS Ctlgrs12592967
GMAF0.4036
Max Magnitude
? (C;C) (C;T) (T;T) 28
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