rs1584157
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1584157(A;A) |
Make rs1584157(A;G) |
Make rs1584157(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 48101263 |
is a | snp |
is | mentioned by |
dbSNP | rs1584157 |
dbSNP (classic) | rs1584157 |
ClinGen | rs1584157 |
ebi | rs1584157 |
HLI | rs1584157 |
Exac | rs1584157 |
Gnomad | rs1584157 |
Varsome | rs1584157 |
LitVar | rs1584157 |
Map | rs1584157 |
PheGenI | rs1584157 |
Biobank | rs1584157 |
1000 genomes | rs1584157 |
hgdp | rs1584157 |
ensembl | rs1584157 |
geneview | rs1584157 |
scholar | rs1584157 |
rs1584157 | |
pharmgkb | rs1584157 |
gwascentral | rs1584157 |
openSNP | rs1584157 |
23andMe | rs1584157 |
SNPshot | rs1584157 |
SNPdbe | rs1584157 |
MSV3d | rs1584157 |
GWAS Ctlg | rs1584157 |
GMAF | 0.2759 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 20125193] non sig. gwas, hit (p = 2 x 10^-6) for forward digit span
GWAS snp | |
---|---|
PMID | [PMID 20125193] |
Trait | Cognitive Performance |
Title | Common genetic variation and performance on standardized cognitive tests |
Risk Allele | |
P-val | 0.000002 |
Odds Ratio | None None |