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

rs939876

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common on affy axiom data
Make rs939876(C;C)
Make rs939876(C;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position64858338
GeneTBC1D30
is asnp
is mentioned by
dbSNPrs939876
dbSNP (classic)rs939876
ClinGenrs939876
ebirs939876
HLIrs939876
Exacrs939876
Gnomadrs939876
Varsomers939876
LitVarrs939876
Maprs939876
PheGenIrs939876
Biobankrs939876
1000 genomesrs939876
hgdprs939876
ensemblrs939876
geneviewrs939876
scholarrs939876
googlers939876
pharmgkbrs939876
gwascentralrs939876
openSNPrs939876
23andMers939876
SNPshotrs939876
SNPdbers939876
MSV3drs939876
GWAS Ctlgrs939876
GMAF0.06382
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 20125193OA-icon.png] non sig. gwas, hit (p = 2 x 10^-6) for Trails B 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 0.000002
Odds Ratio None None