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rs4499362

From SNPedia

Orientationplus
Stabilizedplus
Make rs4499362(C;C)
Make rs4499362(C;T)
Make rs4499362(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position148810827
is asnp
is mentioned by
dbSNPrs4499362
ebirs4499362
HLIrs4499362
Exacrs4499362
Varsomers4499362
Maprs4499362
PheGenIrs4499362
hapmaprs4499362
1000 genomesrs4499362
hgdprs4499362
ensemblrs4499362
gopubmedrs4499362
geneviewrs4499362
scholarrs4499362
googlers4499362
pharmgkbrs4499362
gwascentralrs4499362
openSNPrs4499362
23andMers4499362
23andMe allrs4499362
SNP Nexus

SNPshotrs4499362
SNPdbers4499362
MSV3drs4499362
GWAS Ctlgrs4499362
GMAF0.2929
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21123754OA-icon.png]
Trait
Title Genome-wide association study of CSF biomarkers A{beta}1-42, t-tau, and p-tau181p in the ADNI cohort.
Risk Allele
P-val 0.000001
Odds Ratio None None