rs56109847
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs56109847(A;A) |
| Make rs56109847(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 184106769 |
| Gene | HTR3E, HTR3E-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs56109847 |
| dbSNP (classic) | rs56109847 |
| ClinGen | rs56109847 |
| ebi | rs56109847 |
| HLI | rs56109847 |
| Exac | rs56109847 |
| Gnomad | rs56109847 |
| Varsome | rs56109847 |
| LitVar | rs56109847 |
| Map | rs56109847 |
| PheGenI | rs56109847 |
| Biobank | rs56109847 |
| 1000 genomes | rs56109847 |
| hgdp | rs56109847 |
| ensembl | rs56109847 |
| geneview | rs56109847 |
| scholar | rs56109847 |
| rs56109847 | |
| pharmgkb | rs56109847 |
| gwascentral | rs56109847 |
| openSNP | rs56109847 |
| 23andMe | rs56109847 |
| SNPshot | rs56109847 |
| SNPdbe | rs56109847 |
| MSV3d | rs56109847 |
| GWAS Ctlg | rs56109847 |
| Merged from | Rs62625044 |
| GMAF | 0.01515 |
| Max Magnitude | 0 |
[PMID 18614545] First evidence for an association of a functional variant in the microRNA-510 target site of the serotonin receptor-type 3E gene with diarrhea predominant irritable bowel syndrome.
[PMID 19290790
] MicroRNA polymorphisms: the future of pharmacogenomics, molecular epidemiology and individualized medicine.
[PMID 20428464] MicroRNA polymorphisms: a giant leap towards personalized medicine.
