rs5568
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs5568(A;C) |
| Make rs5568(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 55696212 |
| Gene | SLC6A2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5568 |
| dbSNP (classic) | rs5568 |
| ClinGen | rs5568 |
| ebi | rs5568 |
| HLI | rs5568 |
| Exac | rs5568 |
| Gnomad | rs5568 |
| Varsome | rs5568 |
| LitVar | rs5568 |
| Map | rs5568 |
| PheGenI | rs5568 |
| Biobank | rs5568 |
| 1000 genomes | rs5568 |
| hgdp | rs5568 |
| ensembl | rs5568 |
| geneview | rs5568 |
| scholar | rs5568 |
| rs5568 | |
| pharmgkb | rs5568 |
| gwascentral | rs5568 |
| openSNP | rs5568 |
| 23andMe | rs5568 |
| SNPshot | rs5568 |
| SNPdbe | rs5568 |
| MSV3d | rs5568 |
| GWAS Ctlg | rs5568 |
| GMAF | 0.2755 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
A allele associated with better response to treatment of ADHD with atomoxetine. [PMID 19387424]
[PMID 20863575] Lack of association between response of OROS-methylphenidate and norepinephrine transporter (SLC6A2) polymorphism in Korean ADHD
[PMID 16380908
] Preferential transmission of paternal alleles at risk genes in attention-deficit/hyperactivity disorder.
[PMID 18937309] Sexually dimorphic effects of four genes (COMT, SLC6A2, MAOA, SLC6A4) in genetic associations of ADHD: a preliminary study.
| ClinVar | |
|---|---|
| Risk | rs5568(C;C) |
| Alt | rs5568(C;C) |
| Reference | Rs5568(A;A) |
| Significance | Probable-non-pathogenic |
| Disease | Orthostatic intolerance |
| Variation | info |
| Gene | SLC6A2 |
| CLNDBN | Orthostatic intolerance |
| Reversed | 0 |
| HGVS | NC_000016.9:g.55730124A>C |
| CLNSRC | |
| CLNACC | RCV000336335.1, |
