rs6347
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs6347(A;G) |
| Make rs6347(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 1411297 |
| Gene | SLC6A3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6347 |
| dbSNP (classic) | rs6347 |
| ClinGen | rs6347 |
| ebi | rs6347 |
| HLI | rs6347 |
| Exac | rs6347 |
| Gnomad | rs6347 |
| Varsome | rs6347 |
| LitVar | rs6347 |
| Map | rs6347 |
| PheGenI | rs6347 |
| Biobank | rs6347 |
| 1000 genomes | rs6347 |
| hgdp | rs6347 |
| ensembl | rs6347 |
| geneview | rs6347 |
| scholar | rs6347 |
| rs6347 | |
| pharmgkb | rs6347 |
| gwascentral | rs6347 |
| openSNP | rs6347 |
| 23andMe | rs6347 |
| SNPshot | rs6347 |
| SNPdbe | rs6347 |
| MSV3d | rs6347 |
| GWAS Ctlg | rs6347 |
| GMAF | 0.2989 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19879111] Association of promoter variants of human dopamine transporter gene with schizophrenia in Han Chinese
[PMID 21525861
] Dopamine Transporter Gene Variant Affecting Expression in Human Brain is Associated with Bipolar Disorder
[PMID 16537431] A dopamine transporter gene functional variant associated with cocaine abuse in a Brazilian sample.
[PMID 18698231] Polymorphisms affecting gene transcription and mRNA processing in pharmacogenetic candidate genes: detection through allelic expression imbalance in human target tissues.
[PMID 19183461] SLC6A3 and body mass index in the Prostate, Lung, Colorectal and Ovarian Cancer Screening Trial.
[PMID 19693267] Financial and psychological risk attitudes associated with two single nucleotide polymorphisms in the nicotine receptor (CHRNA4) gene.
[PMID 20445798] Chromosome 5p Region SNPs Are Associated with Risk of NSCLC among Women.
[PMID 23340505] Dopamine transporter DAT and receptor DRD2 variants affect risk of lethal cocaine abuse: a gene-gene-environment interaction
[PMID 22947179] Analysis of 34 candidate genes in bupropion and placebo remission
| ClinVar | |
|---|---|
| Risk | rs6347(G;G) |
| Alt | rs6347(G;G) |
| Reference | Rs6347(A;A) |
| Significance | Non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | SLC6A3 |
| CLNDBN | not specified |
| Reversed | 1 |
| HGVS | NC_000005.9:g.1411412T>C |
| CLNSRC | |
| CLNACC | RCV000180550.1, |
[PMID 28777361] [Associations between chronotype, road accidents and polymorphisms in genes linked with biological clock and dopaminergic system].
