rs13169113
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs13169113(A;A) |
Make rs13169113(A;C) |
Make rs13169113(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 126002782 |
Gene | LOC105379160 |
is a | snp |
is | mentioned by |
dbSNP | rs13169113 |
dbSNP (classic) | rs13169113 |
ClinGen | rs13169113 |
ebi | rs13169113 |
HLI | rs13169113 |
Exac | rs13169113 |
Gnomad | rs13169113 |
Varsome | rs13169113 |
LitVar | rs13169113 |
Map | rs13169113 |
PheGenI | rs13169113 |
Biobank | rs13169113 |
1000 genomes | rs13169113 |
hgdp | rs13169113 |
ensembl | rs13169113 |
geneview | rs13169113 |
scholar | rs13169113 |
rs13169113 | |
pharmgkb | rs13169113 |
gwascentral | rs13169113 |
openSNP | rs13169113 |
23andMe | rs13169113 |
SNPshot | rs13169113 |
SNPdbe | rs13169113 |
MSV3d | rs13169113 |
GWAS Ctlg | rs13169113 |
GMAF | 0.3898 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20125193] |
Trait | Cognitive performance |
Title | Common genetic variation and performance on standardized cognitive tests. |
Risk Allele | |
P-val | 9E-6 |
Odds Ratio | NR NR |