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rs11994034

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common genotype
Make rs11994034(C;T)
Make rs11994034(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position72158500
is asnp
is mentioned by
dbSNPrs11994034
dbSNP (classic)rs11994034
ClinGenrs11994034
ebirs11994034
HLIrs11994034
Exacrs11994034
Gnomadrs11994034
Varsomers11994034
LitVarrs11994034
Maprs11994034
PheGenIrs11994034
Biobankrs11994034
1000 genomesrs11994034
hgdprs11994034
ensemblrs11994034
geneviewrs11994034
scholarrs11994034
googlers11994034
pharmgkbrs11994034
gwascentralrs11994034
openSNPrs11994034
23andMers11994034
SNPshotrs11994034
SNPdbers11994034
MSV3drs11994034
GWAS Ctlgrs11994034
GMAF0.03398
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23527680]
Trait Attention deficit hyperactivity disorder (combined symptoms)
Title Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits.
Risk Allele T
P-val 7E-6
Odds Ratio NR NR