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 |
|---|---|---|
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| ||
[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.
