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rs12146962

From SNPedia

Orientationplus
Stabilizedplus
Make rs12146962(C;C)
Make rs12146962(C;T)
Make rs12146962(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position32911892
is asnp
is mentioned by
dbSNPrs12146962
dbSNP (classic)rs12146962
ClinGenrs12146962
ebirs12146962
HLIrs12146962
Exacrs12146962
Gnomadrs12146962
Varsomers12146962
LitVarrs12146962
Maprs12146962
PheGenIrs12146962
Biobankrs12146962
1000 genomesrs12146962
hgdprs12146962
ensemblrs12146962
geneviewrs12146962
scholarrs12146962
googlers12146962
pharmgkbrs12146962
gwascentralrs12146962
openSNPrs12146962
23andMers12146962
SNPshotrs12146962
SNPdbers12146962
MSV3drs12146962
GWAS Ctlgrs12146962
GMAF0.4252
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 22138694]
Trait
Title A genome-wide association study in Han Chinese identifies new susceptibility loci for ankylosing spondylitis.
Risk Allele
P-val 0.000009
Odds Ratio 1.1400 None