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rs17641078

From SNPedia

Orientationplus
Stabilizedplus
Make rs17641078(C;C)
Make rs17641078(C;G)
Make rs17641078(G;G)
ReferenceGRCh37 37.1/131
Chromosome9
Position1056959
GeneDMRT2
is asnp
is mentioned by
dbSNPrs17641078
ebirs17641078
HLIrs17641078
Exacrs17641078
Varsomers17641078
Maprs17641078
PheGenIrs17641078
hapmaprs17641078
1000 genomesrs17641078
hgdprs17641078
ensemblrs17641078
gopubmedrs17641078
geneviewrs17641078
scholarrs17641078
googlers17641078
pharmgkbrs17641078
gwascentralrs17641078
openSNPrs17641078
23andMers17641078
23andMe allrs17641078
SNP Nexus

SNPshotrs17641078
SNPdbers17641078
MSV3drs17641078
GWAS Ctlgrs17641078
GMAF0.1175
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 18821565]
Trait Hyperactive-impulsive symptoms
Title Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations
Risk Allele
P-val 0.000005
Odds Ratio NR NR


GET Evidence
DMRT2-E458Q
aa_change Glu458Gln
aa_change_short E458Q
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0933259
summary