rs3934492
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3934492(C;C) |
Make rs3934492(C;G) |
Make rs3934492(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 81060164 |
Gene | BAIAP2 |
is a | snp |
is | mentioned by |
dbSNP | rs3934492 |
dbSNP (classic) | rs3934492 |
ClinGen | rs3934492 |
ebi | rs3934492 |
HLI | rs3934492 |
Exac | rs3934492 |
Gnomad | rs3934492 |
Varsome | rs3934492 |
LitVar | rs3934492 |
Map | rs3934492 |
PheGenI | rs3934492 |
Biobank | rs3934492 |
1000 genomes | rs3934492 |
hgdp | rs3934492 |
ensembl | rs3934492 |
geneview | rs3934492 |
scholar | rs3934492 |
rs3934492 | |
pharmgkb | rs3934492 |
gwascentral | rs3934492 |
openSNP | rs3934492 |
23andMe | rs3934492 |
SNPshot | rs3934492 |
SNPdbe | rs3934492 |
MSV3d | rs3934492 |
GWAS Ctlg | rs3934492 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 24377651] BAIAP2 exhibits association to childhood ADHD especially predominantly inattentive subtype in Chinese Han subjects