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rs4764039

From SNPedia

Orientationplus
Stabilizedplus
Make rs4764039(C;C)
Make rs4764039(C;T)
Make rs4764039(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position13911527
GeneGRIN2B
is asnp
is mentioned by
dbSNPrs4764039
ebirs4764039
HLIrs4764039
Exacrs4764039
Varsomers4764039
Maprs4764039
PheGenIrs4764039
hapmaprs4764039
1000 genomesrs4764039
hgdprs4764039
ensemblrs4764039
gopubmedrs4764039
geneviewrs4764039
scholarrs4764039
googlers4764039
pharmgkbrs4764039
gwascentralrs4764039
openSNPrs4764039
23andMers4764039
23andMe allrs4764039
SNP Nexus

SNPshotrs4764039
SNPdbers4764039
MSV3drs4764039
GWAS Ctlgrs4764039
GMAF0.1997
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 0.000003
Odds Ratio 0.0049 [NR] unit increase (main effect)