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rs6119285

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common genotype
Make rs6119285(C;T)
Make rs6119285(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position32789189
GeneDNMT3B
is asnp
is mentioned by
dbSNPrs6119285
dbSNP (classic)rs6119285
ClinGenrs6119285
ebirs6119285
HLIrs6119285
Exacrs6119285
Gnomadrs6119285
Varsomers6119285
LitVarrs6119285
Maprs6119285
PheGenIrs6119285
Biobankrs6119285
1000 genomesrs6119285
hgdprs6119285
ensemblrs6119285
geneviewrs6119285
scholarrs6119285
googlers6119285
pharmgkbrs6119285
gwascentralrs6119285
openSNPrs6119285
23andMers6119285
SNPshotrs6119285
SNPdbers6119285
MSV3drs6119285
GWAS Ctlgrs6119285
GMAF0.1267
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 4E-6
Odds Ratio NR NR