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rs4670766

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs4670766(C;C)
Make rs4670766(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position37713399
is asnp
is mentioned by
dbSNPrs4670766
ebirs4670766
HLIrs4670766
Exacrs4670766
Varsomers4670766
Maprs4670766
PheGenIrs4670766
hapmaprs4670766
1000 genomesrs4670766
hgdprs4670766
ensemblrs4670766
gopubmedrs4670766
geneviewrs4670766
scholarrs4670766
googlers4670766
pharmgkbrs4670766
gwascentralrs4670766
openSNPrs4670766
23andMers4670766
23andMe allrs4670766
SNP Nexus

SNPshotrs4670766
SNPdbers4670766
MSV3drs4670766
GWAS Ctlgrs4670766
GMAF0.1433
Max Magnitude0
? (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 0.000002
Odds Ratio 0.0053 [NR] unit decrease (interaction)