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rs10831284

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0
Make rs10831284(A;G)
Make rs10831284(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position94934799
is asnp
is mentioned by
dbSNPrs10831284
ebirs10831284
HLIrs10831284
Exacrs10831284
Varsomers10831284
Maprs10831284
PheGenIrs10831284
hapmaprs10831284
1000 genomesrs10831284
hgdprs10831284
ensemblrs10831284
gopubmedrs10831284
geneviewrs10831284
scholarrs10831284
googlers10831284
pharmgkbrs10831284
gwascentralrs10831284
openSNPrs10831284
23andMers10831284
23andMe allrs10831284
SNP Nexus

SNPshotrs10831284
SNPdbers10831284
MSV3drs10831284
GWAS Ctlgrs10831284
GMAF0.208
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 18951430]
Trait Attention-deficit/hyperactivity disorder and conduct disorder
Title Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study
Risk Allele G
P-val 0.000002
Odds Ratio NR NR


The G allele of rs10831284 is associated with a higher risk of attention deficit hyperactivity disorder (ADHD) and conduct disorder. [PMID 18951430]


GET Evidence
rs10831284
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.695312
summary