rs12000567
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12000567(A;A) |
Make rs12000567(A;C) |
Make rs12000567(C;C) |
Reference | GRCh38 38.1/142 |
Chromosome | 9 |
Position | 789499 |
is a | snp |
is | mentioned by |
dbSNP | rs12000567 |
dbSNP (classic) | rs12000567 |
ClinGen | rs12000567 |
ebi | rs12000567 |
HLI | rs12000567 |
Exac | rs12000567 |
Gnomad | rs12000567 |
Varsome | rs12000567 |
LitVar | rs12000567 |
Map | rs12000567 |
PheGenI | rs12000567 |
Biobank | rs12000567 |
1000 genomes | rs12000567 |
hgdp | rs12000567 |
ensembl | rs12000567 |
geneview | rs12000567 |
scholar | rs12000567 |
rs12000567 | |
pharmgkb | rs12000567 |
gwascentral | rs12000567 |
openSNP | rs12000567 |
23andMe | rs12000567 |
SNPshot | rs12000567 |
SNPdbe | rs12000567 |
MSV3d | rs12000567 |
GWAS Ctlg | rs12000567 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24839885] |
Trait | Preschool internalizing problems |
Title | A genome-wide association meta-analysis of preschool internalizing problems. |
Risk Allele | A |
P-val | 8E-6 |
Odds Ratio | .63 [0.35-0.91] unit increase |