rs7448069
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7448069(C;C) |
Make rs7448069(C;T) |
Make rs7448069(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 175817031 |
Gene | CPLX2 |
is a | snp |
is | mentioned by |
dbSNP | rs7448069 |
dbSNP (classic) | rs7448069 |
ClinGen | rs7448069 |
ebi | rs7448069 |
HLI | rs7448069 |
Exac | rs7448069 |
Gnomad | rs7448069 |
Varsome | rs7448069 |
LitVar | rs7448069 |
Map | rs7448069 |
PheGenI | rs7448069 |
Biobank | rs7448069 |
1000 genomes | rs7448069 |
hgdp | rs7448069 |
ensembl | rs7448069 |
geneview | rs7448069 |
scholar | rs7448069 |
rs7448069 | |
pharmgkb | rs7448069 |
gwascentral | rs7448069 |
openSNP | rs7448069 |
23andMe | rs7448069 |
SNPshot | rs7448069 |
SNPdbe | rs7448069 |
MSV3d | rs7448069 |
GWAS Ctlg | rs7448069 |
GMAF | 0.02663 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23527680] |
Trait | Attention deficit hyperactivity disorder (inattention symptoms) |
Title | Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits. |
Risk Allele | T |
P-val | 1E-6 |
Odds Ratio | NR NR |