Have questions? Visit https://www.reddit.com/r/SNPedia

rs10767942

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs10767942(C;C)
Make rs10767942(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position32500461
GeneLOC101059934
is asnp
is mentioned by
dbSNPrs10767942
ebirs10767942
HLIrs10767942
Exacrs10767942
Varsomers10767942
Maprs10767942
PheGenIrs10767942
hapmaprs10767942
1000 genomesrs10767942
hgdprs10767942
ensemblrs10767942
gopubmedrs10767942
geneviewrs10767942
scholarrs10767942
googlers10767942
pharmgkbrs10767942
gwascentralrs10767942
openSNPrs10767942
23andMers10767942
23andMe allrs10767942
SNP Nexus

SNPshotrs10767942
SNPdbers10767942
MSV3drs10767942
GWAS Ctlgrs10767942
GMAF0.3646
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18821565]
Trait Attention deficit hyperactivity disorder
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 0.000008
Odds Ratio NR NR


GET Evidence
rs10767942
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.351562
summary