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rs9471576

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs9471576(A;A)
Make rs9471576(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position41336067
GeneNCR2
is asnp
is mentioned by
dbSNPrs9471576
ebirs9471576
HLIrs9471576
Exacrs9471576
Varsomers9471576
Maprs9471576
PheGenIrs9471576
hapmaprs9471576
1000 genomesrs9471576
hgdprs9471576
ensemblrs9471576
gopubmedrs9471576
geneviewrs9471576
scholarrs9471576
googlers9471576
pharmgkbrs9471576
gwascentralrs9471576
openSNPrs9471576
23andMers9471576
23andMe allrs9471576
SNP Nexus

SNPshotrs9471576
SNPdbers9471576
MSV3drs9471576
GWAS Ctlgrs9471576
GMAF0.1671
Max Magnitude0
? (A;A) (A;G) (G;G) 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 0.0093 [NR] unit increase (main effect)