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rs6057648

From SNPedia

Orientationplus
Stabilizedplus
Make rs6057648(A;A)
Make rs6057648(A;C)
Make rs6057648(C;C)
ReferenceGRCh38 38.1/141
Chromosome20
Position32797074
GeneDNMT3B
is asnp
is mentioned by
dbSNPrs6057648
dbSNP (classic)rs6057648
ClinGenrs6057648
ebirs6057648
HLIrs6057648
Exacrs6057648
Gnomadrs6057648
Varsomers6057648
LitVarrs6057648
Maprs6057648
PheGenIrs6057648
Biobankrs6057648
1000 genomesrs6057648
hgdprs6057648
ensemblrs6057648
geneviewrs6057648
scholarrs6057648
googlers6057648
pharmgkbrs6057648
gwascentralrs6057648
openSNPrs6057648
23andMers6057648
SNPshotrs6057648
SNPdbers6057648
MSV3drs6057648
GWAS Ctlgrs6057648
GMAF0.05739
Max Magnitude0
? (A;A) (A;C) (C;C) 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 A
P-val 4E-6
Odds Ratio NR NR