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rs11687170

From SNPedia

Orientationplus
Stabilizedplus
Make rs11687170(C;C)
Make rs11687170(C;T)
Make rs11687170(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position236149500
is asnp
is mentioned by
dbSNPrs11687170
ebirs11687170
HLIrs11687170
Exacrs11687170
Varsomers11687170
Maprs11687170
PheGenIrs11687170
hapmaprs11687170
1000 genomesrs11687170
hgdprs11687170
ensemblrs11687170
gopubmedrs11687170
geneviewrs11687170
scholarrs11687170
googlers11687170
pharmgkbrs11687170
gwascentralrs11687170
openSNPrs11687170
23andMers11687170
23andMe allrs11687170
SNP Nexus

SNPshotrs11687170
SNPdbers11687170
MSV3drs11687170
GWAS Ctlgrs11687170
GMAF0.1639
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 3E-8
Odds Ratio .11 [NR] unit increase