rs6766410
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6766410(A;A) |
| Make rs6766410(A;C) |
| Make rs6766410(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 184056974 |
| Gene | HTR3C |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6766410 |
| dbSNP (classic) | rs6766410 |
| ClinGen | rs6766410 |
| ebi | rs6766410 |
| HLI | rs6766410 |
| Exac | rs6766410 |
| Gnomad | rs6766410 |
| Varsome | rs6766410 |
| LitVar | rs6766410 |
| Map | rs6766410 |
| PheGenI | rs6766410 |
| Biobank | rs6766410 |
| 1000 genomes | rs6766410 |
| hgdp | rs6766410 |
| ensembl | rs6766410 |
| geneview | rs6766410 |
| scholar | rs6766410 |
| rs6766410 | |
| pharmgkb | rs6766410 |
| gwascentral | rs6766410 |
| openSNP | rs6766410 |
| 23andMe | rs6766410 |
| SNPshot | rs6766410 |
| SNPdbe | rs6766410 |
| MSV3d | rs6766410 |
| GWAS Ctlg | rs6766410 |
| GMAF | 0.4949 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
rs6766410 is a SNP in the 5-hydroxytryptamine (serotonin) receptor 3, family member C HTR3C gene.
In a study of 97 familes with at least one individual with autism, rs6766410 was significantly associated with the disorder (p = 0.0012).[PMID 19035560
]
[PMID 23928294] 5-HT3 receptor influences the washing phenotype and visual organization in obsessive-compulsive disorder supporting 5-HT3 receptor antagonists as novel treatment option
