Have questions? Visit https://www.reddit.com/r/SNPedia

rs5568

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs5568(A;C)
Make rs5568(C;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position55696212
GeneSLC6A2
is asnp
is mentioned by
dbSNPrs5568
dbSNP (classic)rs5568
ClinGenrs5568
ebirs5568
HLIrs5568
Exacrs5568
Gnomadrs5568
Varsomers5568
LitVarrs5568
Maprs5568
PheGenIrs5568
Biobankrs5568
1000 genomesrs5568
hgdprs5568
ensemblrs5568
geneviewrs5568
scholarrs5568
googlers5568
pharmgkbrs5568
gwascentralrs5568
openSNPrs5568
23andMers5568
SNPshotrs5568
SNPdbers5568
MSV3drs5568
GWAS Ctlgrs5568
GMAF0.2755
Max Magnitude0
? (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 16380908OA-icon.png] Preferential transmission of paternal alleles at risk genes in attention-deficit/hyperactivity disorder.


[PMID 18937309OA-icon.png] 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,