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rs6739054

From SNPedia

Orientationplus
Stabilizedplus
Make rs6739054(A;A)
Make rs6739054(A;G)
Make rs6739054(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position11080436
is asnp
is mentioned by
dbSNPrs6739054
dbSNP (classic)rs6739054
ClinGenrs6739054
ebirs6739054
HLIrs6739054
Exacrs6739054
Gnomadrs6739054
Varsomers6739054
LitVarrs6739054
Maprs6739054
PheGenIrs6739054
Biobankrs6739054
1000 genomesrs6739054
hgdprs6739054
ensemblrs6739054
geneviewrs6739054
scholarrs6739054
googlers6739054
pharmgkbrs6739054
gwascentralrs6739054
openSNPrs6739054
23andMers6739054
SNPshotrs6739054
SNPdbers6739054
MSV3drs6739054
GWAS Ctlgrs6739054
GMAF0.3017
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 20125193OA-icon.png] non sig. gwas, hit (p = 2 x 10^-6) for PC1 (principal component 1) among the cognitive tests performed

GWAS snp
PMID [PMID 20125193OA-icon.png]
Trait Cognitive Performance
Title Common genetic variation and performance on standardized cognitive tests
Risk Allele
P-val 0.000002
Odds Ratio None None