rs3785152
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs3785152(C;T) |
Make rs3785152(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 55682638 |
Gene | SLC6A2 |
is a | snp |
is | mentioned by |
dbSNP | rs3785152 |
dbSNP (classic) | rs3785152 |
ClinGen | rs3785152 |
ebi | rs3785152 |
HLI | rs3785152 |
Exac | rs3785152 |
Gnomad | rs3785152 |
Varsome | rs3785152 |
LitVar | rs3785152 |
Map | rs3785152 |
PheGenI | rs3785152 |
Biobank | rs3785152 |
1000 genomes | rs3785152 |
hgdp | rs3785152 |
ensembl | rs3785152 |
geneview | rs3785152 |
scholar | rs3785152 |
rs3785152 | |
pharmgkb | rs3785152 |
gwascentral | rs3785152 |
openSNP | rs3785152 |
23andMe | rs3785152 |
SNPshot | rs3785152 |
SNPdbe | rs3785152 |
MSV3d | rs3785152 |
GWAS Ctlg | rs3785152 |
GMAF | 0.1249 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
T allele associated with better response to treatment of ADHD with atomoxetine. [PMID 19387424]
[PMID 18937309] Sexually dimorphic effects of four genes (COMT, SLC6A2, MAOA, SLC6A4) in genetic associations of ADHD: a preliminary study.