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rs931812

From SNPedia

Orientationplus
Stabilizedplus
Make rs931812(C;C)
Make rs931812(C;T)
Make rs931812(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position100907093
is asnp
is mentioned by
dbSNPrs931812
ClinGenrs931812
ebirs931812
HLIrs931812
Exacrs931812
Varsomers931812
Maprs931812
PheGenIrs931812
hapmaprs931812
1000 genomesrs931812
hgdprs931812
ensemblrs931812
gopubmedrs931812
geneviewrs931812
scholarrs931812
googlers931812
pharmgkbrs931812
gwascentralrs931812
openSNPrs931812
23andMers931812
23andMe allrs931812
SNP Nexus

SNPshotrs931812
SNPdbers931812
MSV3drs931812
GWAS Ctlgrs931812
GMAF0.2314
Max Magnitude
? (C;C) (C;T) (T;T) 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 C
P-val 0.000005
Odds Ratio NR NR



GET Evidence
rs931812
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.1875
summary