rs3784962
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3784962(A;A) |
Make rs3784962(A;G) |
Make rs3784962(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 83723723 |
Gene | CDH13, LOC105371366 |
is a | snp |
is | mentioned by |
dbSNP | rs3784962 |
dbSNP (classic) | rs3784962 |
ClinGen | rs3784962 |
ebi | rs3784962 |
HLI | rs3784962 |
Exac | rs3784962 |
Gnomad | rs3784962 |
Varsome | rs3784962 |
LitVar | rs3784962 |
Map | rs3784962 |
PheGenI | rs3784962 |
Biobank | rs3784962 |
1000 genomes | rs3784962 |
hgdp | rs3784962 |
ensembl | rs3784962 |
geneview | rs3784962 |
scholar | rs3784962 |
rs3784962 | |
pharmgkb | rs3784962 |
gwascentral | rs3784962 |
openSNP | rs3784962 |
23andMe | rs3784962 |
SNPshot | rs3784962 |
SNPdbe | rs3784962 |
MSV3d | rs3784962 |
GWAS Ctlg | rs3784962 |
GMAF | 0.3673 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 20125193] non sig. gwas, hit (p = 3 x 10^-6) for Trails B performance
GWAS snp | |
---|---|
PMID | [PMID 20125193] |
Trait | Cognitive Performance |
Title | Common genetic variation and performance on standardized cognitive tests |
Risk Allele | |
P-val | 0.000003 |
Odds Ratio | None None |