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rs1265564

From SNPedia

Orientationplus
Stabilizedplus
Make rs1265564(A;A)
Make rs1265564(A;C)
Make rs1265564(C;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position111270654
GeneCUX2
is asnp
is mentioned by
dbSNPrs1265564
ebirs1265564
HLIrs1265564
Exacrs1265564
Varsomers1265564
Maprs1265564
PheGenIrs1265564
hapmaprs1265564
1000 genomesrs1265564
hgdprs1265564
ensemblrs1265564
gopubmedrs1265564
geneviewrs1265564
scholarrs1265564
googlers1265564
pharmgkbrs1265564
gwascentralrs1265564
openSNPrs1265564
23andMers1265564
23andMe allrs1265564
SNP Nexus

SNPshotrs1265564
SNPdbers1265564
MSV3drs1265564
GWAS Ctlgrs1265564
GMAF0.1933
Max Magnitude
GWAS snp
PMID [PMID 22293688OA-icon.png]
Trait
Title 1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data.
Risk Allele
P-val 1E-16
Odds Ratio 1.4500 None