Have questions? Visit https://www.reddit.com/r/SNPedia

rs4861096

From SNPedia

Orientationplus
Stabilizedplus
Make rs4861096(C;C)
Make rs4861096(C;T)
Make rs4861096(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position41282694
is asnp
is mentioned by
dbSNPrs4861096
ebirs4861096
HLIrs4861096
Exacrs4861096
Varsomers4861096
Maprs4861096
PheGenIrs4861096
hapmaprs4861096
1000 genomesrs4861096
hgdprs4861096
ensemblrs4861096
gopubmedrs4861096
geneviewrs4861096
scholarrs4861096
googlers4861096
pharmgkbrs4861096
gwascentralrs4861096
openSNPrs4861096
23andMers4861096
23andMe allrs4861096
SNP Nexus

SNPshotrs4861096
SNPdbers4861096
MSV3drs4861096
GWAS Ctlgrs4861096
GMAF0.2695
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19734545OA-icon.png]
Trait Cognitive performance
Title A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.
Risk Allele
P-val 9E-6
Odds Ratio NR NR