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rs1079596

From SNPedia

Orientationminus
Stabilizedminus
Make rs1079596(A;A)
Make rs1079596(A;G)
Make rs1079596(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position113425897
GeneDRD2
is asnp
is mentioned by
dbSNPrs1079596
ebirs1079596
HLIrs1079596
Exacrs1079596
Varsomers1079596
Maprs1079596
PheGenIrs1079596
hapmaprs1079596
1000 genomesrs1079596
hgdprs1079596
ensemblrs1079596
gopubmedrs1079596
geneviewrs1079596
scholarrs1079596
googlers1079596
pharmgkbrs1079596
gwascentralrs1079596
openSNPrs1079596
23andMers1079596
23andMe allrs1079596
SNP Nexus

SNPshotrs1079596
SNPdbers1079596
MSV3drs1079596
GWAS Ctlgrs1079596
GMAF0.2332
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 17903293OA-icon.png]
Trait Select biomarker traits
Title Genome-wide association with select biomarker traits in the Framingham Heart Study
Risk Allele
P-val 0.0000030000000000000001
Odds Ratio NR NR


[PMID 18821566OA-icon.png] SNPs in dopamine D2 receptor gene (DRD2) and norepinephrine transporter gene (NET) are associated with continuous performance task (CPT) phenotypes in ADHD children and their families.


[PMID 19968402OA-icon.png] Evaluation of genetic variability in the dopamine receptor D2 in relation to behavioral inhibition and impulsivity/sensation seeking: an exploratory study with d-amphetamine in healthy participants.


GET Evidence
rs1079596
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.265625
summary