Rs6807362
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6807362 |
| PheGenI | rs6807362 |
| nextbio | rs6807362 |
| hapmap | rs6807362 |
| 1000 genomes | rs6807362 |
| hgdp | rs6807362 |
| ensembl | rs6807362 |
| gopubmed | rs6807362 |
| geneview | rs6807362 |
| scholar | rs6807362 |
| rs6807362 | |
| pharmgkb | rs6807362 |
| gwascentral | rs6807362 |
| openSNP | rs6807362 |
| 23andMe | rs6807362 |
| 23andMe all | rs6807362 |
| SNP Nexus | |
| SNPshot | rs6807362 |
| SNPdbe | rs6807362 |
| MSV3d | rs6807362 |
| Gene | HTR3C |
| Chromosome | 3 |
| Orientation | plus |
| GMAF | 0.4057 |
| Position | 183778010 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude |
| Make rs6807362(C;C) |
| Make rs6807362(C;G) |
| Make rs6807362(G;G) |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
In a study of 97 familes with at least one individual with autism, rs6807362 was significantly associated with the disorder (p = 0.0012).[PMID 19035560]
| GET Evidence | |
|---|---|
| HTR3C-G405A | |
| aa_change | Gly405Ala |
| aa_change_short | G405A |
| impact | not reviewed |
| qualified_impact | Insufficiently evaluated not reviewed |
| overall_frequency | 0.511154 |
| summary | |
