Rs6766410
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6766410 |
| PheGenI | rs6766410 |
| nextbio | rs6766410 |
| hapmap | rs6766410 |
| 1000 genomes | rs6766410 |
| hgdp | rs6766410 |
| ensembl | rs6766410 |
| gopubmed | rs6766410 |
| geneview | rs6766410 |
| scholar | rs6766410 |
| rs6766410 | |
| pharmgkb | rs6766410 |
| gwascentral | rs6766410 |
| openSNP | rs6766410 |
| 23andMe | rs6766410 |
| 23andMe all | rs6766410 |
| SNP Nexus | |
| SNPshot | rs6766410 |
| SNPdbe | rs6766410 |
| MSV3d | rs6766410 |
| Gene | HTR3C |
| Chromosome | 3 |
| Orientation | plus |
| GMAF | 0.495 |
| Position | 183774762 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude |
| Make rs6766410(A;A) |
| Make rs6766410(A;C) |
| Make rs6766410(C;C) |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
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]
| GET Evidence | |
|---|---|
| HTR3C-N163K | |
| aa_change | Asn163Lys |
| aa_change_short | N163K |
| impact | not reviewed |
| qualified_impact | Insufficiently evaluated not reviewed |
| overall_frequency | 0.423685 |
| summary | |
