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rs10879517

From SNPedia

Orientationplus
Stabilizedplus
Make rs10879517(A;A)
Make rs10879517(A;G)
Make rs10879517(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position72913802
is asnp
is mentioned by
dbSNPrs10879517
dbSNP (classic)rs10879517
ClinGenrs10879517
ebirs10879517
HLIrs10879517
Exacrs10879517
Gnomadrs10879517
Varsomers10879517
LitVarrs10879517
Maprs10879517
PheGenIrs10879517
Biobankrs10879517
1000 genomesrs10879517
hgdprs10879517
ensemblrs10879517
geneviewrs10879517
scholarrs10879517
googlers10879517
pharmgkbrs10879517
gwascentralrs10879517
openSNPrs10879517
23andMers10879517
SNPshotrs10879517
SNPdbers10879517
MSV3drs10879517
GWAS Ctlgrs10879517
GMAF0.2443
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 20125193OA-icon.png] non sig. gwas, hit (p = 4 x 10^-6) for Trails A performance

GWAS snp
PMID [PMID 20125193OA-icon.png]
Trait Cognitive Performance
Title Common genetic variation and performance on standardized cognitive tests
Risk Allele
P-val 0.000004
Odds Ratio None None