Have questions? Visit https://www.reddit.com/r/SNPedia

rs11564750

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs11564750(C;G)
Make rs11564750(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position1447647
is asnp
is mentioned by
dbSNPrs11564750
ebirs11564750
HLIrs11564750
Exacrs11564750
Varsomers11564750
Maprs11564750
PheGenIrs11564750
hapmaprs11564750
1000 genomesrs11564750
hgdprs11564750
ensemblrs11564750
gopubmedrs11564750
geneviewrs11564750
scholarrs11564750
googlers11564750
pharmgkbrs11564750
gwascentralrs11564750
openSNPrs11564750
23andMers11564750
23andMe allrs11564750
SNP Nexus

SNPshotrs11564750
SNPdbers11564750
MSV3drs11564750
GWAS Ctlgrs11564750
GMAF0.04224
Max Magnitude0

[PMID 19576958]Replication of an association of a promoter polymorphism of the dopamine transporter gene and Attention Deficit Hyperactivity Disorder.

[PMID 18668530]Association of ADHD with genetic variants in the 5'-region of the dopamine transporter gene: evidence for allelic heterogeneity.

[PMID 16894395]The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes.

GET Evidence
rs11564750
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.015625
summary