Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3836790
rs3836790
SLC6A3
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 GeneticVariation BEFREE Analysis of the genotypes of SLC6A3-MS8 (rs3836790) revealed that having an 8/6-repeat allele, which was only detected in hypertensive cases, was associated with hypertension (p < 0.05). 28055236

2017
dbSNP: rs3836790
rs3836790
SLC6A3
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.010 GeneticVariation BEFREE Our data suggest that variants rs28363170 and rs3836790 are not associated with sporadic PD in Han Chinese population. 27353511

2016
dbSNP: rs3836790
rs3836790
SLC6A3
CUI: C4511452
Disease: Sporadic Parkinson disease
Sporadic Parkinson disease 		0.010 GeneticVariation BEFREE SLC6A3 rs28363170 and rs3836790 variants in Han Chinese patients with sporadic Parkinson's disease. 27353511

2016
dbSNP: rs3836790
rs3836790
SLC6A3
CUI: C0424295
Disease: Hyperactive behavior
Hyperactive behavior 		0.010 GeneticVariation BEFREE We explored association of functional variants in the DA receptor 2 (rs1799732 and rs6278), receptor 4 (exon 3 VNTR and rs914655), and transporter (rs28363170 and rs3836790) with hyperactivity, cognitive deficit, and co-morbid disorders in eastern Indian probands. 24585059

2014
dbSNP: rs3836790
rs3836790
SLC6A3
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.010 GeneticVariation BEFREE MDR analyses revealed independent effects of rs1799732, rs6278, rs914655, and rs3836790 in ADHD. 24585059

2014