rs11642377
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11642377(A;A) |
Make rs11642377(A;G) |
Make rs11642377(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 20098331 |
is a | snp |
is | mentioned by |
dbSNP | rs11642377 |
dbSNP (classic) | rs11642377 |
ClinGen | rs11642377 |
ebi | rs11642377 |
HLI | rs11642377 |
Exac | rs11642377 |
Gnomad | rs11642377 |
Varsome | rs11642377 |
LitVar | rs11642377 |
Map | rs11642377 |
PheGenI | rs11642377 |
Biobank | rs11642377 |
1000 genomes | rs11642377 |
hgdp | rs11642377 |
ensembl | rs11642377 |
geneview | rs11642377 |
scholar | rs11642377 |
rs11642377 | |
pharmgkb | rs11642377 |
gwascentral | rs11642377 |
openSNP | rs11642377 |
23andMe | rs11642377 |
SNPshot | rs11642377 |
SNPdbe | rs11642377 |
MSV3d | rs11642377 |
GWAS Ctlg | rs11642377 |
GMAF | 0.2029 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 |