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rs1569476

From SNPedia

Orientationminus
Stabilizedminus
Make rs1569476(A;A)
Make rs1569476(A;G)
Make rs1569476(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position169639679
is asnp
is mentioned by
dbSNPrs1569476
ebirs1569476
HLIrs1569476
Exacrs1569476
Varsomers1569476
Maprs1569476
PheGenIrs1569476
hapmaprs1569476
1000 genomesrs1569476
hgdprs1569476
ensemblrs1569476
gopubmedrs1569476
geneviewrs1569476
scholarrs1569476
googlers1569476
pharmgkbrs1569476
gwascentralrs1569476
openSNPrs1569476
23andMers1569476
23andMe allrs1569476
SNP Nexus

SNPshotrs1569476
SNPdbers1569476
MSV3drs1569476
GWAS Ctlgrs1569476
GMAF0.2888
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 3E-7
Odds Ratio 0.0032 [NR] unit increase (main effect)