Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3785143
rs3785143
Entrez Id: 6530
Gene Symbol: SLC6A2
SLC6A2
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder
0.030 GeneticVariation BEFREE In the present genetic association study three single nucleotide polymorphisms (rs28386840, rs2242446, rs3785143 SNPs) were analyzed from the 5' region of the norepinephrine transporter (<i>NET</i>, <i>SLC6A2</i>) gene, which have been linked to ADHD previously. 30692908 2018
dbSNP: rs3785143
rs3785143
Entrez Id: 6530
Gene Symbol: SLC6A2
SLC6A2
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder
0.030 GeneticVariation BEFREE As a result, we found association of the same alleles from two single-nucleotide polymorphisms (rs3785143 and rs11568324) previously identified in another large-scale ADHD genetic study (International Multisite ADHD Geneproject). 17876324 2008
dbSNP: rs3785143
rs3785143
Entrez Id: 6530
Gene Symbol: SLC6A2
SLC6A2
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder
0.030 GeneticVariation BEFREE However, across all four datasets the overall evidence of association with ADHD was significant (for SNP rs11568324 P = 0.0001; average odds ratio = 0.33; for SNP rs3785143 P = 0.008; average odds ratio = 1.3). 18937296 2008