rs3785157
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3785157(C;C) |
Make rs3785157(C;T) |
Make rs3785157(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 55695924 |
Gene | SLC6A2 |
is a | snp |
is | mentioned by |
dbSNP | rs3785157 |
dbSNP (classic) | rs3785157 |
ClinGen | rs3785157 |
ebi | rs3785157 |
HLI | rs3785157 |
Exac | rs3785157 |
Gnomad | rs3785157 |
Varsome | rs3785157 |
LitVar | rs3785157 |
Map | rs3785157 |
PheGenI | rs3785157 |
Biobank | rs3785157 |
1000 genomes | rs3785157 |
hgdp | rs3785157 |
ensembl | rs3785157 |
geneview | rs3785157 |
scholar | rs3785157 |
rs3785157 | |
pharmgkb | rs3785157 |
gwascentral | rs3785157 |
openSNP | rs3785157 |
23andMe | rs3785157 |
SNPshot | rs3785157 |
SNPdbe | rs3785157 |
MSV3d | rs3785157 |
GWAS Ctlg | rs3785157 |
GMAF | 0.2557 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
Support for association between ADHD and two candidate genes: NET1 and DRD1.[PMID 15717291]
[PMID 18937296] Replication of a rare protective allele in the noradrenaline transporter gene and ADHD.
[PMID 18937309] Sexually dimorphic effects of four genes (COMT, SLC6A2, MAOA, SLC6A4) in genetic associations of ADHD: a preliminary study.
[PMID 25724484] Association of norepinephrine transporter (NET, SLC6A2) genotype with ADHD-related phenotypes: Findings of a longitudinal study from birth to adolescence
[PMID 27230021] Testing for the mediating role of endophenotypes using molecular genetic data in a twin study of ADHD traits.