rs6296
Orientation | minus |
Stabilized | minus |
Make rs6296(C;C) |
Make rs6296(C;G) |
Make rs6296(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 77462543 |
Gene | HTR1B, LOC105377864 |
is a | snp |
is | mentioned by |
dbSNP | rs6296 |
dbSNP (classic) | rs6296 |
ClinGen | rs6296 |
ebi | rs6296 |
HLI | rs6296 |
Exac | rs6296 |
Gnomad | rs6296 |
Varsome | rs6296 |
LitVar | rs6296 |
Map | rs6296 |
PheGenI | rs6296 |
Biobank | rs6296 |
1000 genomes | rs6296 |
hgdp | rs6296 |
ensembl | rs6296 |
geneview | rs6296 |
scholar | rs6296 |
rs6296 | |
pharmgkb | rs6296 |
gwascentral | rs6296 |
openSNP | rs6296 |
23andMe | rs6296 |
SNPshot | rs6296 |
SNPdbe | rs6296 |
MSV3d | rs6296 |
GWAS Ctlg | rs6296 |
GMAF | 0.3526 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 22005095] A haplotype analysis is consistent with the role of functional HTR1B variants in alcohol dependence
[PMID 19506906] Candidate gene studies of ADHD: a meta-analytic review
[PMID 17938636] Exploration of 19 serotoninergic candidate genes in adults and children with attention-deficit/hyperactivity disorder identifies association for 5HT2A, DDC and MAOB
[PMID 1619792] Association between the 5HT1B receptor gene (HTR1B) and the inattentive subtype of ADHD
[PMID 15206000] Transmission disequilibrium studies in children and adolescents with obsessive-compulsive disorders pertaining to polymorphisms of genes of the serotonergic pathway.
[PMID 16380908] Preferential transmission of paternal alleles at risk genes in attention-deficit/hyperactivity disorder.
[PMID 17948897] Association of 5-HT1B receptor polymorphisms with the loudness dependence of auditory evoked potentials in a community-based sample of healthy volunteers.
[PMID 18698231] Polymorphisms affecting gene transcription and mRNA processing in pharmacogenetic candidate genes: detection through allelic expression imbalance in human target tissues.
[PMID 19350534] Functional polymorphisms in the serotonin 1B receptor gene (HTR1B) predict self-reported anger and hostility among young men.
[PMID 19379518] Development of a fingerprinting panel using medically relevant polymorphisms.
[PMID 19721846] Candidate genes involved in neural plasticity and the risk for attention-deficit hyperactivity disorder: a meta-analysis of 8 common variants.
[PMID 20388441] [Association study of HTR1A and HTR1B with adolescent idiopathic scoliosis].
[PMID 20565774] Population based allele frequencies of disease associated polymorphisms in the Personalized Medicine Research Project.
[PMID 20638825] The HTR1A and HTR1B receptor genes influence stress-related information processing.
[PMID 21937687] Influence and interaction of genetic polymorphisms in the serotonin system and life stress on antidepressant drug response.
[PMID 22735397] Serotonin system gene polymorphisms are associated with impulsivity in a context dependent manner.
[PMID 22841130] Shared and unique genetic contributions to attention deficit/hyperactivity disorder and substance use disorders: a pilot study of six candidate genes.
[PMID 22945537] Serotonin receptor 1B genotype and hostility, anger and aggressive behavior through the lifespan: the Young Finns study.
[PMID 23375453] Genetic association of 5-HT1A and 5-HT1B gene polymorphisms with migraine in a Turkish population.
[PMID 25652393] Interaction between 5-HTTLPR and 5-HT1B genotype status enhances cerebral 5-HT1A receptor binding
[PMID 30074224] Association of Serotonin Receptors with Attention Deficit Hyperactivity Disorder: A Systematic Review and Meta-analysis.
[PMID 30700110] Genetic Variants and the Cortisol Response in Children: An Exploratory Study.