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rs4851266

From SNPedia

Orientationplus
Stabilizedplus
Make rs4851266(C;C)
Make rs4851266(C;T)
Make rs4851266(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position100202017
is asnp
is mentioned by
dbSNPrs4851266
ebirs4851266
HLIrs4851266
Exacrs4851266
Varsomers4851266
Maprs4851266
PheGenIrs4851266
hapmaprs4851266
1000 genomesrs4851266
hgdprs4851266
ensemblrs4851266
gopubmedrs4851266
geneviewrs4851266
scholarrs4851266
googlers4851266
pharmgkbrs4851266
gwascentralrs4851266
openSNPrs4851266
23andMers4851266
23andMe allrs4851266
SNP Nexus

SNPshotrs4851266
SNPdbers4851266
MSV3drs4851266
GWAS Ctlgrs4851266
GMAF0.3292
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23722424OA-icon.png]
Trait Educational attainment
Title GWAS of 126,559 individuals identifies genetic variants associated with educational attainment.
Risk Allele T
P-val 5E-11
Odds Ratio 1.05 [NR]