rs4450776
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common on affy axiom data |
Make rs4450776(C;G) |
Make rs4450776(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 111704282 |
Gene | PLCXD2 |
is a | snp |
is | mentioned by |
dbSNP | rs4450776 |
dbSNP (classic) | rs4450776 |
ClinGen | rs4450776 |
ebi | rs4450776 |
HLI | rs4450776 |
Exac | rs4450776 |
Gnomad | rs4450776 |
Varsome | rs4450776 |
LitVar | rs4450776 |
Map | rs4450776 |
PheGenI | rs4450776 |
Biobank | rs4450776 |
1000 genomes | rs4450776 |
hgdp | rs4450776 |
ensembl | rs4450776 |
geneview | rs4450776 |
scholar | rs4450776 |
rs4450776 | |
pharmgkb | rs4450776 |
gwascentral | rs4450776 |
openSNP | rs4450776 |
23andMe | rs4450776 |
SNPshot | rs4450776 |
SNPdbe | rs4450776 |
MSV3d | rs4450776 |
GWAS Ctlg | rs4450776 |
GMAF | 0.06428 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 20125193] non sig. gwas, hit (p = 5 x 10^-6) for PC1 (principal component 1) among the cognitive tests performed
GWAS snp | |
---|---|
PMID | [PMID 20125193![]() |
Trait | Cognitive Performance |
Title | Common genetic variation and performance on standardized cognitive tests |
Risk Allele | |
P-val | 0.000005 |
Odds Ratio | None None |