rs4969385
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4969385(C;C) |
Make rs4969385(C;T) |
Make rs4969385(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 81095090 |
Gene | BAIAP2 |
is a | snp |
is | mentioned by |
dbSNP | rs4969385 |
dbSNP (classic) | rs4969385 |
ClinGen | rs4969385 |
ebi | rs4969385 |
HLI | rs4969385 |
Exac | rs4969385 |
Gnomad | rs4969385 |
Varsome | rs4969385 |
LitVar | rs4969385 |
Map | rs4969385 |
PheGenI | rs4969385 |
Biobank | rs4969385 |
1000 genomes | rs4969385 |
hgdp | rs4969385 |
ensembl | rs4969385 |
geneview | rs4969385 |
scholar | rs4969385 |
rs4969385 | |
pharmgkb | rs4969385 |
gwascentral | rs4969385 |
openSNP | rs4969385 |
23andMe | rs4969385 |
SNPshot | rs4969385 |
SNPdbe | rs4969385 |
MSV3d | rs4969385 |
GWAS Ctlg | rs4969385 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 24377651] BAIAP2 exhibits association to childhood ADHD especially predominantly inattentive subtype in Chinese Han subjects