rs492478
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs492478(A;A) |
Make rs492478(A;G) |
Make rs492478(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 3939362 |
is a | snp |
is | mentioned by |
dbSNP | rs492478 |
dbSNP (classic) | rs492478 |
ClinGen | rs492478 |
ebi | rs492478 |
HLI | rs492478 |
Exac | rs492478 |
Gnomad | rs492478 |
Varsome | rs492478 |
LitVar | rs492478 |
Map | rs492478 |
PheGenI | rs492478 |
Biobank | rs492478 |
1000 genomes | rs492478 |
hgdp | rs492478 |
ensembl | rs492478 |
geneview | rs492478 |
scholar | rs492478 |
rs492478 | |
pharmgkb | rs492478 |
gwascentral | rs492478 |
openSNP | rs492478 |
23andMe | rs492478 |
SNPshot | rs492478 |
SNPdbe | rs492478 |
MSV3d | rs492478 |
GWAS Ctlg | rs492478 |
GMAF | 0.1983 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 20125193] non sig. gwas, hit (p = 4 x 10^-6) for Stroop test performance
GWAS snp | |
---|---|
PMID | [PMID 20125193] |
Trait | Cognitive Performance |
Title | Common genetic variation and performance on standardized cognitive tests |
Risk Allele | |
P-val | 0.000004 |
Odds Ratio | None None |