rs4810796
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4810796(A;A) |
Make rs4810796(A;G) |
Make rs4810796(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 48459954 |
is a | snp |
is | mentioned by |
dbSNP | rs4810796 |
dbSNP (classic) | rs4810796 |
ClinGen | rs4810796 |
ebi | rs4810796 |
HLI | rs4810796 |
Exac | rs4810796 |
Gnomad | rs4810796 |
Varsome | rs4810796 |
LitVar | rs4810796 |
Map | rs4810796 |
PheGenI | rs4810796 |
Biobank | rs4810796 |
1000 genomes | rs4810796 |
hgdp | rs4810796 |
ensembl | rs4810796 |
geneview | rs4810796 |
scholar | rs4810796 |
rs4810796 | |
pharmgkb | rs4810796 |
gwascentral | rs4810796 |
openSNP | rs4810796 |
23andMe | rs4810796 |
SNPshot | rs4810796 |
SNPdbe | rs4810796 |
MSV3d | rs4810796 |
GWAS Ctlg | rs4810796 |
GMAF | 0.3994 |
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 | 3E-6 |
Odds Ratio | NR NR |