rs5941436
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common on affy axiom data |
Make rs5941436(A;A) |
Make rs5941436(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 90033228 |
is a | snp |
is | mentioned by |
dbSNP | rs5941436 |
dbSNP (classic) | rs5941436 |
ClinGen | rs5941436 |
ebi | rs5941436 |
HLI | rs5941436 |
Exac | rs5941436 |
Gnomad | rs5941436 |
Varsome | rs5941436 |
LitVar | rs5941436 |
Map | rs5941436 |
PheGenI | rs5941436 |
Biobank | rs5941436 |
1000 genomes | rs5941436 |
hgdp | rs5941436 |
ensembl | rs5941436 |
geneview | rs5941436 |
scholar | rs5941436 |
rs5941436 | |
pharmgkb | rs5941436 |
gwascentral | rs5941436 |
openSNP | rs5941436 |
23andMe | rs5941436 |
SNPshot | rs5941436 |
SNPdbe | rs5941436 |
MSV3d | rs5941436 |
GWAS Ctlg | rs5941436 |
GMAF | 0.1838 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 20125193] non sig. gwas, hit (p = 5 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 | 0.000005 |
Odds Ratio | None None |