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rs1876040

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs1876040(C;C)
Make rs1876040(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position18953470
is asnp
is mentioned by
dbSNPrs1876040
ebirs1876040
HLIrs1876040
Exacrs1876040
Varsomers1876040
Maprs1876040
PheGenIrs1876040
hapmaprs1876040
1000 genomesrs1876040
hgdprs1876040
ensemblrs1876040
gopubmedrs1876040
geneviewrs1876040
scholarrs1876040
googlers1876040
pharmgkbrs1876040
gwascentralrs1876040
openSNPrs1876040
23andMers1876040
23andMe allrs1876040
SNP Nexus

SNPshotrs1876040
SNPdbers1876040
MSV3drs1876040
GWAS Ctlgrs1876040
GMAF0.1469
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 20125193OA-icon.png] non sig. gwas, hit (p = 6 x 10^-8) for backwards digit span
GWAS snp
PMID [PMID 20125193OA-icon.png]
Trait Cognitive Performance
Title Common genetic variation and performance on standardized cognitive tests
Risk Allele
P-val 6E-8
Odds Ratio None None