rs9901648
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9901648(A;A) |
Make rs9901648(A;G) |
Make rs9901648(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 81061908 |
Gene | BAIAP2 |
is a | snp |
is | mentioned by |
dbSNP | rs9901648 |
dbSNP (classic) | rs9901648 |
ClinGen | rs9901648 |
ebi | rs9901648 |
HLI | rs9901648 |
Exac | rs9901648 |
Gnomad | rs9901648 |
Varsome | rs9901648 |
LitVar | rs9901648 |
Map | rs9901648 |
PheGenI | rs9901648 |
Biobank | rs9901648 |
1000 genomes | rs9901648 |
hgdp | rs9901648 |
ensembl | rs9901648 |
geneview | rs9901648 |
scholar | rs9901648 |
rs9901648 | |
pharmgkb | rs9901648 |
gwascentral | rs9901648 |
openSNP | rs9901648 |
23andMe | rs9901648 |
SNPshot | rs9901648 |
SNPdbe | rs9901648 |
MSV3d | rs9901648 |
GWAS Ctlg | rs9901648 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 24377651] BAIAP2 exhibits association to childhood ADHD especially predominantly inattentive subtype in Chinese Han subjects