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rs4298437

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0
Make rs4298437(C;T)
Make rs4298437(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position103985430
GeneRELN
is asnp
is mentioned by
dbSNPrs4298437
ebirs4298437
HLIrs4298437
Exacrs4298437
Varsomers4298437
Maprs4298437
PheGenIrs4298437
hapmaprs4298437
1000 genomesrs4298437
hgdprs4298437
ensemblrs4298437
gopubmedrs4298437
geneviewrs4298437
scholarrs4298437
googlers4298437
pharmgkbrs4298437
gwascentralrs4298437
openSNPrs4298437
23andMers4298437
23andMe allrs4298437
SNP Nexus

SNPshotrs4298437
SNPdbers4298437
MSV3drs4298437
GWAS Ctlgrs4298437
GMAF0.2346
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20452100OA-icon.png]
Trait Alzheimer's disease
Title Alzheimer disease pathology in cognitively healthy elderly: A genome-wide study
Risk Allele
P-val 0.000002
Odds Ratio None None

The risk allele is T (in dbSNP orientation), according to a table published by the National Human Genome Research Institute.