rs3773679
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3773679(A;A) |
Make rs3773679(A;G) |
Make rs3773679(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 3 |
Position | 114150488 |
Gene | DRD3 |
is a | snp |
is | mentioned by |
dbSNP | rs3773679 |
dbSNP (classic) | rs3773679 |
ClinGen | rs3773679 |
ebi | rs3773679 |
HLI | rs3773679 |
Exac | rs3773679 |
Gnomad | rs3773679 |
Varsome | rs3773679 |
LitVar | rs3773679 |
Map | rs3773679 |
PheGenI | rs3773679 |
Biobank | rs3773679 |
1000 genomes | rs3773679 |
hgdp | rs3773679 |
ensembl | rs3773679 |
geneview | rs3773679 |
scholar | rs3773679 |
rs3773679 | |
pharmgkb | rs3773679 |
gwascentral | rs3773679 |
openSNP | rs3773679 |
23andMe | rs3773679 |
SNPshot | rs3773679 |
SNPdbe | rs3773679 |
MSV3d | rs3773679 |
GWAS Ctlg | rs3773679 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 26254621] Association between genetic variants related to glutamatergic, dopaminergic and neurodevelopment pathways and white matter microstructure in child and adolescent patients with obsessive-compulsive disorder