rs7627615
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7627615(A;A) |
| Make rs7627615(A;G) |
| Make rs7627615(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 184100628 |
| Gene | HTR3E, HTR3E-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7627615 |
| dbSNP (classic) | rs7627615 |
| ClinGen | rs7627615 |
| ebi | rs7627615 |
| HLI | rs7627615 |
| Exac | rs7627615 |
| Gnomad | rs7627615 |
| Varsome | rs7627615 |
| LitVar | rs7627615 |
| Map | rs7627615 |
| PheGenI | rs7627615 |
| Biobank | rs7627615 |
| 1000 genomes | rs7627615 |
| hgdp | rs7627615 |
| ensembl | rs7627615 |
| geneview | rs7627615 |
| scholar | rs7627615 |
| rs7627615 | |
| pharmgkb | rs7627615 |
| gwascentral | rs7627615 |
| openSNP | rs7627615 |
| 23andMe | rs7627615 |
| SNPshot | rs7627615 |
| SNPdbe | rs7627615 |
| MSV3d | rs7627615 |
| GWAS Ctlg | rs7627615 |
| GMAF | 0.2548 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20356718] A coding variant of the novel serotonin receptor subunit 5-HT3E influences sustained attention in schizophrenia patients
[PMID 18710563
] A human genome-wide library of local phylogeny predictions for whole-genome inference problems.
[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
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 3
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
