rs11647507
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11647507(A;A) |
Make rs11647507(A;C) |
Make rs11647507(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 20084306 |
is a | snp |
is | mentioned by |
dbSNP | rs11647507 |
dbSNP (classic) | rs11647507 |
ClinGen | rs11647507 |
ebi | rs11647507 |
HLI | rs11647507 |
Exac | rs11647507 |
Gnomad | rs11647507 |
Varsome | rs11647507 |
LitVar | rs11647507 |
Map | rs11647507 |
PheGenI | rs11647507 |
Biobank | rs11647507 |
1000 genomes | rs11647507 |
hgdp | rs11647507 |
ensembl | rs11647507 |
geneview | rs11647507 |
scholar | rs11647507 |
rs11647507 | |
pharmgkb | rs11647507 |
gwascentral | rs11647507 |
openSNP | rs11647507 |
23andMe | rs11647507 |
SNPshot | rs11647507 |
SNPdbe | rs11647507 |
MSV3d | rs11647507 |
GWAS Ctlg | rs11647507 |
GMAF | 0.2039 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 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 | A |
P-val | 7E-6 |
Odds Ratio | NR NR |