rs10455248
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10455248(C;C) |
Make rs10455248(C;T) |
Make rs10455248(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 71772755 |
is a | snp |
is | mentioned by |
dbSNP | rs10455248 |
dbSNP (classic) | rs10455248 |
ClinGen | rs10455248 |
ebi | rs10455248 |
HLI | rs10455248 |
Exac | rs10455248 |
Gnomad | rs10455248 |
Varsome | rs10455248 |
LitVar | rs10455248 |
Map | rs10455248 |
PheGenI | rs10455248 |
Biobank | rs10455248 |
1000 genomes | rs10455248 |
hgdp | rs10455248 |
ensembl | rs10455248 |
geneview | rs10455248 |
scholar | rs10455248 |
rs10455248 | |
pharmgkb | rs10455248 |
gwascentral | rs10455248 |
openSNP | rs10455248 |
23andMe | rs10455248 |
SNPshot | rs10455248 |
SNPdbe | rs10455248 |
MSV3d | rs10455248 |
GWAS Ctlg | rs10455248 |
GMAF | 0.191 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20125193] non sig. gwas, hit (p = 4 x 10^-6) for Trails A performance
GWAS snp | |
---|---|
PMID | [PMID 20125193] |
Trait | Cognitive Performance |
Title | Common genetic variation and performance on standardized cognitive tests |
Risk Allele | |
P-val | 0.000004 |
Odds Ratio | None None |