rs1923886
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1923886(C;C) |
Make rs1923886(C;T) |
Make rs1923886(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 46849156 |
Gene | HTR2A |
is a | snp |
is | mentioned by |
dbSNP | rs1923886 |
dbSNP (classic) | rs1923886 |
ClinGen | rs1923886 |
ebi | rs1923886 |
HLI | rs1923886 |
Exac | rs1923886 |
Gnomad | rs1923886 |
Varsome | rs1923886 |
LitVar | rs1923886 |
Map | rs1923886 |
PheGenI | rs1923886 |
Biobank | rs1923886 |
1000 genomes | rs1923886 |
hgdp | rs1923886 |
ensembl | rs1923886 |
geneview | rs1923886 |
scholar | rs1923886 |
rs1923886 | |
pharmgkb | rs1923886 |
gwascentral | rs1923886 |
openSNP | rs1923886 |
23andMe | rs1923886 |
SNPshot | rs1923886 |
SNPdbe | rs1923886 |
MSV3d | rs1923886 |
GWAS Ctlg | rs1923886 |
GMAF | 0.3623 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 19584773] Association between the serotonin 2A receptor gene and bipolar affective disorder in an Australian cohort
- "Haplotype association analysis suggests that the haplotype CCGCA (at SNPs rs3125, rs6314, rs1923886, rs2224721 and rs2770296) is protective against bipolar disorder (P = 0.021, odds ratio 0.63) and the rarer haplotype CCACG confers risk to the disorder (P = 0.0065, odds ratio 3.08)."
[PMID 18937842] The influence of serotonin- and other genes on impulsive behavioral aggression and cognitive impulsivity in children with attention-deficit/hyperactivity disorder (ADHD): Findings from a family-based association test (FBAT) analysis.