rs4975646
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4975646(A;A) |
Make rs4975646(A;G) |
Make rs4975646(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 5 |
Position | 1433286 |
Gene | SLC6A3 |
is a | snp |
is | mentioned by |
dbSNP | rs4975646 |
dbSNP (classic) | rs4975646 |
ClinGen | rs4975646 |
ebi | rs4975646 |
HLI | rs4975646 |
Exac | rs4975646 |
Gnomad | rs4975646 |
Varsome | rs4975646 |
LitVar | rs4975646 |
Map | rs4975646 |
PheGenI | rs4975646 |
Biobank | rs4975646 |
1000 genomes | rs4975646 |
hgdp | rs4975646 |
ensembl | rs4975646 |
geneview | rs4975646 |
scholar | rs4975646 |
rs4975646 | |
pharmgkb | rs4975646 |
gwascentral | rs4975646 |
openSNP | rs4975646 |
23andMe | rs4975646 |
SNPshot | rs4975646 |
SNPdbe | rs4975646 |
MSV3d | rs4975646 |
GWAS Ctlg | rs4975646 |
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