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rs2506933

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs2506933(C;C)
Make rs2506933(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position92905732
is asnp
is mentioned by
dbSNPrs2506933
ebirs2506933
HLIrs2506933
Exacrs2506933
Varsomers2506933
Maprs2506933
PheGenIrs2506933
hapmaprs2506933
1000 genomesrs2506933
hgdprs2506933
ensemblrs2506933
gopubmedrs2506933
geneviewrs2506933
scholarrs2506933
googlers2506933
pharmgkbrs2506933
gwascentralrs2506933
openSNPrs2506933
23andMers2506933
23andMe allrs2506933
SNP Nexus

SNPshotrs2506933
SNPdbers2506933
MSV3drs2506933
GWAS Ctlgrs2506933
GMAF0.2388
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 20125193OA-icon.png] non sig. gwas, hit (p = 6 x 10^-6) - Animals
GWAS snp
PMID [PMID 20125193OA-icon.png]
Trait Cognitive Performance
Title Common genetic variation and performance on standardized cognitive tests
Risk Allele
P-val 0.000006
Odds Ratio None None