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rs12555345

From SNPedia

Orientationplus
Stabilizedplus
Make rs12555345(C;C)
Make rs12555345(C;T)
Make rs12555345(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position27630564
GeneCTAGE12P
is asnp
is mentioned by
dbSNPrs12555345
ebirs12555345
HLIrs12555345
Exacrs12555345
Varsomers12555345
Maprs12555345
PheGenIrs12555345
hapmaprs12555345
1000 genomesrs12555345
hgdprs12555345
ensemblrs12555345
gopubmedrs12555345
geneviewrs12555345
scholarrs12555345
googlers12555345
pharmgkbrs12555345
gwascentralrs12555345
openSNPrs12555345
23andMers12555345
23andMe allrs12555345
SNP Nexus

SNPshotrs12555345
SNPdbers12555345
MSV3drs12555345
GWAS Ctlgrs12555345
GMAF0.2374
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21116278]
Trait
Title Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease
Risk Allele
P-val 0.000005
Odds Ratio 0.0039 [NR] unit decrease (interaction)