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rs4937314

From SNPedia

Orientationplus
Stabilizedplus
Make rs4937314(A;A)
Make rs4937314(A;G)
Make rs4937314(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position128319206
is asnp
is mentioned by
dbSNPrs4937314
ebirs4937314
HLIrs4937314
Exacrs4937314
Varsomers4937314
Maprs4937314
PheGenIrs4937314
hapmaprs4937314
1000 genomesrs4937314
hgdprs4937314
ensemblrs4937314
gopubmedrs4937314
geneviewrs4937314
scholarrs4937314
googlers4937314
pharmgkbrs4937314
gwascentralrs4937314
openSNPrs4937314
23andMers4937314
23andMe allrs4937314
SNP Nexus

SNPshotrs4937314
SNPdbers4937314
MSV3drs4937314
GWAS Ctlgrs4937314
GMAF0.1657
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22881374OA-icon.png]
Trait Alzheimer's disease (late onset)
Title Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene.
Risk Allele C
P-val 7E-6
Odds Ratio NR NR