rs28914832
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs28914832(A;G) |
| Make rs28914832(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 30211356 |
| Gene | SLC6A4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs28914832 |
| dbSNP (classic) | rs28914832 |
| ClinGen | rs28914832 |
| ebi | rs28914832 |
| HLI | rs28914832 |
| Exac | rs28914832 |
| Gnomad | rs28914832 |
| Varsome | rs28914832 |
| LitVar | rs28914832 |
| Map | rs28914832 |
| PheGenI | rs28914832 |
| Biobank | rs28914832 |
| 1000 genomes | rs28914832 |
| hgdp | rs28914832 |
| ensembl | rs28914832 |
| geneview | rs28914832 |
| scholar | rs28914832 |
| rs28914832 | |
| pharmgkb | rs28914832 |
| gwascentral | rs28914832 |
| openSNP | rs28914832 |
| 23andMe | rs28914832 |
| SNPshot | rs28914832 |
| SNPdbe | rs28914832 |
| MSV3d | rs28914832 |
| GWAS Ctlg | rs28914832 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs28914832(C;C) rs28914832(G;G) |
| Alt | rs28914832(C;C) rs28914832(G;G) |
| Reference | Rs28914832(A;A) |
| Significance | Other |
| Disease | Obsessive-compulsive disorder |
| Variation | info |
| Gene | SLC6A4 |
| CLNDBN | Obsessive-compulsive disorder, susceptibility to |
| Reversed | 1 |
| HGVS | NC_000017.10:g.28538374T>C |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000013798.2, |
[PMID 15995945
] Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors.
[PMID 18957375] Enhanced activity of human serotonin transporter variants associated with autism.
[PMID 19032574] Characterization of a functional polymorphism in the 3' UTR of SLC6A4 and its association with drinking intensity.
