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rs969962

From SNPedia

Orientationplus
Stabilizedplus
Make rs969962(C;C)
Make rs969962(C;T)
Make rs969962(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position88110091
is asnp
is mentioned by
dbSNPrs969962
ebirs969962
HLIrs969962
Exacrs969962
Varsomers969962
Maprs969962
PheGenIrs969962
hapmaprs969962
1000 genomesrs969962
hgdprs969962
ensemblrs969962
gopubmedrs969962
geneviewrs969962
scholarrs969962
googlers969962
pharmgkbrs969962
gwascentralrs969962
openSNPrs969962
23andMers969962
23andMe allrs969962
SNP Nexus

SNPshotrs969962
SNPdbers969962
MSV3drs969962
GWAS Ctlgrs969962
GMAF0.1529
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