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rs4450776

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs4450776(C;G)
Make rs4450776(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position111704282
GenePLCXD2
is asnp
is mentioned by
dbSNPrs4450776
dbSNP (classic)rs4450776
ClinGenrs4450776
ebirs4450776
HLIrs4450776
Exacrs4450776
Gnomadrs4450776
Varsomers4450776
LitVarrs4450776
Maprs4450776
PheGenIrs4450776
Biobankrs4450776
1000 genomesrs4450776
hgdprs4450776
ensemblrs4450776
geneviewrs4450776
scholarrs4450776
googlers4450776
pharmgkbrs4450776
gwascentralrs4450776
openSNPrs4450776
23andMers4450776
SNPshotrs4450776
SNPdbers4450776
MSV3drs4450776
GWAS Ctlgrs4450776
GMAF0.06428
Max Magnitude0
? (C;C) (C;G) (G;G) 28


[PMID 20125193OA-icon.png] non sig. gwas, hit (p = 5 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 0.000005
Odds Ratio None None