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rs9846480

From SNPedia

Orientationplus
Stabilizedplus
Make rs9846480(A;A)
Make rs9846480(A;G)
Make rs9846480(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position138306554
GeneNME9
is asnp
is mentioned by
dbSNPrs9846480
ebirs9846480
HLIrs9846480
Exacrs9846480
Varsomers9846480
Maprs9846480
PheGenIrs9846480
hapmaprs9846480
1000 genomesrs9846480
hgdprs9846480
ensemblrs9846480
gopubmedrs9846480
geneviewrs9846480
scholarrs9846480
googlers9846480
pharmgkbrs9846480
gwascentralrs9846480
openSNPrs9846480
23andMers9846480
23andMe allrs9846480
SNP Nexus

SNPshotrs9846480
SNPdbers9846480
MSV3drs9846480
GWAS Ctlgrs9846480
GMAF0.404
Max Magnitude
? (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 0.000008
Odds Ratio 0.0085 [NR] unit increase (interaction)