rs7782376
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs7782376(A;A) |
Make rs7782376(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 116937070 |
is a | snp |
is | mentioned by |
dbSNP | rs7782376 |
dbSNP (classic) | rs7782376 |
ClinGen | rs7782376 |
ebi | rs7782376 |
HLI | rs7782376 |
Exac | rs7782376 |
Gnomad | rs7782376 |
Varsome | rs7782376 |
LitVar | rs7782376 |
Map | rs7782376 |
PheGenI | rs7782376 |
Biobank | rs7782376 |
1000 genomes | rs7782376 |
hgdp | rs7782376 |
ensembl | rs7782376 |
geneview | rs7782376 |
scholar | rs7782376 |
rs7782376 | |
pharmgkb | rs7782376 |
gwascentral | rs7782376 |
openSNP | rs7782376 |
23andMe | rs7782376 |
SNPshot | rs7782376 |
SNPdbe | rs7782376 |
MSV3d | rs7782376 |
GWAS Ctlg | rs7782376 |
GMAF | 0.3747 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 20125193] non sig. gwas, hit (p = 8 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 | 0.000008 |
Odds Ratio | None None |