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rs998424

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs998424(C;T)
Make rs998424(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position55698034
GeneSLC6A2
is asnp
is mentioned by
dbSNPrs998424
dbSNP (classic)rs998424
ClinGenrs998424
ebirs998424
HLIrs998424
Exacrs998424
Gnomadrs998424
Varsomers998424
LitVarrs998424
Maprs998424
PheGenIrs998424
Biobankrs998424
1000 genomesrs998424
hgdprs998424
ensemblrs998424
geneviewrs998424
scholarrs998424
googlers998424
pharmgkbrs998424
gwascentralrs998424
openSNPrs998424
23andMers998424
SNPshotrs998424
SNPdbers998424
MSV3drs998424
GWAS Ctlgrs998424
GMAF0.2681
Max Magnitude0

[PMID 17994190] Norepinephrine transporter and catecholamine-O-methyltransferase gene variants and attention-deficit/hyperactivity disorder symptoms in adults.

[PMID 17876324]Further evidence of association between two NET single-nucleotide polymorphisms with ADHD.

[PMID 20863575]Lack of association between response of OROS-methylphenidate and norepinephrine transporter (SLC6A2) polymorphism in Korean ADHD.

[PMID 21122117OA-icon.png] Genetic influences on attention deficit hyperactivity disorder symptoms from age 2 to 3: a quantitative and molecular genetic investigation.

[PMID 15717291] Support for association between ADHD and two candidate genes: NET1 and DRD1.


[PMID 18937296OA-icon.png] Replication of a rare protective allele in the noradrenaline transporter gene and ADHD.


[PMID 18937309OA-icon.png] Sexually dimorphic effects of four genes (COMT, SLC6A2, MAOA, SLC6A4) in genetic associations of ADHD: a preliminary study.


[PMID 19693267OA-icon.png] Financial and psychological risk attitudes associated with two single nucleotide polymorphisms in the nicotine receptor (CHRNA4) gene.


[PMID 19721846OA-icon.png] Candidate genes involved in neural plasticity and the risk for attention-deficit hyperactivity disorder: a meta-analysis of 8 common variants.


ClinVar
Risk rs998424(T;T)
Alt rs998424(T;T)
Reference Rs998424(C;C)
Significance Probable-non-pathogenic
Disease Orthostatic intolerance
Variation info
Gene SLC6A2
CLNDBN Orthostatic intolerance
Reversed 1
HGVS NC_000016.9:g.55731946G>A
CLNSRC
CLNACC RCV000358821.1,