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rs3785152

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs3785152(C;T)
Make rs3785152(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position55682638
GeneSLC6A2
is asnp
is mentioned by
dbSNPrs3785152
ebirs3785152
HLIrs3785152
Exacrs3785152
Varsomers3785152
Maprs3785152
PheGenIrs3785152
hapmaprs3785152
1000 genomesrs3785152
hgdprs3785152
ensemblrs3785152
gopubmedrs3785152
geneviewrs3785152
scholarrs3785152
googlers3785152
pharmgkbrs3785152
gwascentralrs3785152
openSNPrs3785152
23andMers3785152
23andMe allrs3785152
SNP Nexus

SNPshotrs3785152
SNPdbers3785152
MSV3drs3785152
GWAS Ctlgrs3785152
GMAF0.1249
Max Magnitude0
? (C;C) (C;T) (T;T) 28
T allele associated with better response to treatment of ADHD with atomoxetine. [PMID 19387424]


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