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rs472926

From SNPedia

Orientationminus
Stabilizedminus
Make rs472926(A;A)
Make rs472926(A;G)
Make rs472926(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position126035363
GeneCDON
is asnp
is mentioned by
dbSNPrs472926
dbSNP (classic)rs472926
ClinGenrs472926
ebirs472926
HLIrs472926
Exacrs472926
Gnomadrs472926
Varsomers472926
LitVarrs472926
Maprs472926
PheGenIrs472926
Biobankrs472926
1000 genomesrs472926
hgdprs472926
ensemblrs472926
geneviewrs472926
scholarrs472926
googlers472926
pharmgkbrs472926
gwascentralrs472926
openSNPrs472926
23andMers472926
SNPshotrs472926
SNPdbers472926
MSV3drs472926
GWAS Ctlgrs472926
GMAF0.1442
Max Magnitude0
? (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 3E-6
Odds Ratio NR NR