rs7984966
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7984966(C;C) |
Make rs7984966(C;T) |
Make rs7984966(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 46855311 |
Gene | HTR2A, HTR2A-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs7984966 |
dbSNP (classic) | rs7984966 |
ClinGen | rs7984966 |
ebi | rs7984966 |
HLI | rs7984966 |
Exac | rs7984966 |
Gnomad | rs7984966 |
Varsome | rs7984966 |
LitVar | rs7984966 |
Map | rs7984966 |
PheGenI | rs7984966 |
Biobank | rs7984966 |
1000 genomes | rs7984966 |
hgdp | rs7984966 |
ensembl | rs7984966 |
geneview | rs7984966 |
scholar | rs7984966 |
rs7984966 | |
pharmgkb | rs7984966 |
gwascentral | rs7984966 |
openSNP | rs7984966 |
23andMe | rs7984966 |
SNPshot | rs7984966 |
SNPdbe | rs7984966 |
MSV3d | rs7984966 |
GWAS Ctlg | rs7984966 |
GMAF | 0.2144 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
Exploration of 19 serotoninergic candidate genes in adults and children with attention-deficit/hyperactivity disorder identifies association for 5HT2A, DDC and MAOB. C allele associated with ADHD in adults.
[PMID 27230021] Testing for the mediating role of endophenotypes using molecular genetic data in a twin study of ADHD traits.
This study's data while replicating the association of rs7984966 with ADHD behaviors, instead points to the 'T' allele as being the cause.