rs6050267
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6050267(A;A) |
Make rs6050267(A;G) |
Make rs6050267(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 25038463 |
Gene | ACSS1 |
is a | snp |
is | mentioned by |
dbSNP | rs6050267 |
dbSNP (classic) | rs6050267 |
ClinGen | rs6050267 |
ebi | rs6050267 |
HLI | rs6050267 |
Exac | rs6050267 |
Gnomad | rs6050267 |
Varsome | rs6050267 |
LitVar | rs6050267 |
Map | rs6050267 |
PheGenI | rs6050267 |
Biobank | rs6050267 |
1000 genomes | rs6050267 |
hgdp | rs6050267 |
ensembl | rs6050267 |
geneview | rs6050267 |
scholar | rs6050267 |
rs6050267 | |
pharmgkb | rs6050267 |
gwascentral | rs6050267 |
openSNP | rs6050267 |
23andMe | rs6050267 |
SNPshot | rs6050267 |
SNPdbe | rs6050267 |
MSV3d | rs6050267 |
GWAS Ctlg | rs6050267 |
GMAF | 0.14 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 |