rs10879517
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10879517(A;A) |
Make rs10879517(A;G) |
Make rs10879517(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 72913802 |
is a | snp |
is | mentioned by |
dbSNP | rs10879517 |
dbSNP (classic) | rs10879517 |
ClinGen | rs10879517 |
ebi | rs10879517 |
HLI | rs10879517 |
Exac | rs10879517 |
Gnomad | rs10879517 |
Varsome | rs10879517 |
LitVar | rs10879517 |
Map | rs10879517 |
PheGenI | rs10879517 |
Biobank | rs10879517 |
1000 genomes | rs10879517 |
hgdp | rs10879517 |
ensembl | rs10879517 |
geneview | rs10879517 |
scholar | rs10879517 |
rs10879517 | |
pharmgkb | rs10879517 |
gwascentral | rs10879517 |
openSNP | rs10879517 |
23andMe | rs10879517 |
SNPshot | rs10879517 |
SNPdbe | rs10879517 |
MSV3d | rs10879517 |
GWAS Ctlg | rs10879517 |
GMAF | 0.2443 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 20125193] non sig. gwas, hit (p = 4 x 10^-6) for Trails A 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 |