rs11681930
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11681930(A;A) |
Make rs11681930(A;G) |
Make rs11681930(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 205198574 |
Gene | PARD3B |
is a | snp |
is | mentioned by |
dbSNP | rs11681930 |
dbSNP (classic) | rs11681930 |
ClinGen | rs11681930 |
ebi | rs11681930 |
HLI | rs11681930 |
Exac | rs11681930 |
Gnomad | rs11681930 |
Varsome | rs11681930 |
LitVar | rs11681930 |
Map | rs11681930 |
PheGenI | rs11681930 |
Biobank | rs11681930 |
1000 genomes | rs11681930 |
hgdp | rs11681930 |
ensembl | rs11681930 |
geneview | rs11681930 |
scholar | rs11681930 |
rs11681930 | |
pharmgkb | rs11681930 |
gwascentral | rs11681930 |
openSNP | rs11681930 |
23andMe | rs11681930 |
SNPshot | rs11681930 |
SNPdbe | rs11681930 |
MSV3d | rs11681930 |
GWAS Ctlg | rs11681930 |
GMAF | 0.2709 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23527680] |
Trait | Attention deficit hyperactivity disorder (combined symptoms) |
Title | Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits. |
Risk Allele | A |
P-val | 5E-6 |
Odds Ratio | NR NR |