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rs181500

From SNPedia

Orientationminus
Stabilizedminus
Make rs181500(A;A)
Make rs181500(A;C)
Make rs181500(C;C)
ReferenceGRCh38 38.1/142
Chromosome10
Position117422360
is asnp
is mentioned by
dbSNPrs181500
ebirs181500
HLIrs181500
Exacrs181500
Varsomers181500
Maprs181500
PheGenIrs181500
hapmaprs181500
1000 genomesrs181500
hgdprs181500
ensemblrs181500
gopubmedrs181500
geneviewrs181500
scholarrs181500
googlers181500
pharmgkbrs181500
gwascentralrs181500
openSNPrs181500
23andMers181500
23andMe allrs181500
SNP Nexus

SNPshotrs181500
SNPdbers181500
MSV3drs181500
GWAS Ctlgrs181500
GMAF0.3838
Max Magnitude
? (A;A) (A;C) (C;C) 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 T
P-val 0.000005
Odds Ratio 1.2400 None