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rs40184

From SNPedia

Orientationminus
Stabilizedminus
Make rs40184(A;A)
Make rs40184(A;G)
Make rs40184(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position1394962
GeneSLC6A3
is asnp
is mentioned by
dbSNPrs40184
dbSNP (classic)rs40184
ClinGenrs40184
ebirs40184
HLIrs40184
Exacrs40184
Gnomadrs40184
Varsomers40184
LitVarrs40184
Maprs40184
PheGenIrs40184
Biobankrs40184
1000 genomesrs40184
hgdprs40184
ensemblrs40184
geneviewrs40184
scholarrs40184
googlers40184
pharmgkbrs40184
gwascentralrs40184
openSNPrs40184
23andMers40184
SNPshotrs40184
SNPdbers40184
MSV3drs40184
GWAS Ctlgrs40184
GMAF0.405
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 20391341] Association of C/T polymorphism in intron 14 of the dopamine transporter gene (rs40184) with major depression in a northeastern Thai population


[PMID 16848906OA-icon.png] Genetic polymorphisms in monoamine neurotransmitter systems show only weak association with acute post-surgical pain in humans.


[PMID 17526637] D2 dopamine receptor gene haplotypes and their influence on alcohol and tobacco consumption magnitude in alcohol-dependent individuals.


[PMID 18181793] Association between polymorphisms in the dopamine transporter gene and depression: evidence for a gene-environment interaction in a sample of juvenile detainees.


[PMID 18361424] Family based association study of pediatric bipolar disorder and the dopamine transporter gene (SLC6A3).


[PMID 18553640] Genetic heterogeneity in ADHD: DAT1 gene only affects probands without CD.


[PMID 19152006] New genetic evidence for involvement of the dopamine system in migraine with aura.


[PMID 19673036OA-icon.png] Association of tagging single nucleotide polymorphisms on 8 candidate genes in dopaminergic pathway with schizophrenia in Croatian population.


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


[PMID 19772578OA-icon.png] Two-stage case-control association study of dopamine-related genes and migraine.


[PMID 31565212OA-icon.png] Variants in the 3' End of SLC6A3 in Northwest Han Population with Parkinson's.