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rs9611198

From SNPedia

Orientationplus
Stabilizedplus
Make rs9611198(A;A)
Make rs9611198(A;C)
Make rs9611198(C;C)
ReferenceGRCh38 38.1/141
Chromosome22
Position39559868
is asnp
is mentioned by
dbSNPrs9611198
ebirs9611198
HLIrs9611198
Exacrs9611198
Varsomers9611198
Maprs9611198
PheGenIrs9611198
hapmaprs9611198
1000 genomesrs9611198
hgdprs9611198
ensemblrs9611198
gopubmedrs9611198
geneviewrs9611198
scholarrs9611198
googlers9611198
pharmgkbrs9611198
gwascentralrs9611198
openSNPrs9611198
23andMers9611198
23andMe allrs9611198
SNP Nexus

SNPshotrs9611198
SNPdbers9611198
MSV3drs9611198
GWAS Ctlgrs9611198
GMAF0.3104
Max Magnitude
GWAS snp
PMID [PMID 22883433OA-icon.png]
Trait Schizophrenia
Title Genome-wide association study implicates HLA-C*01:02 as a risk factor at the major histocompatibility complex locus in schizophrenia.
Risk Allele C
P-val 8E-6
Odds Ratio 1.22 [1.11-1.34]