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rs6733379

From SNPedia

Orientationplus
Stabilizedplus
Make rs6733379(G;G)
Make rs6733379(G;T)
Make rs6733379(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position34255008
is asnp
is mentioned by
dbSNPrs6733379
ebirs6733379
HLIrs6733379
Exacrs6733379
Varsomers6733379
Maprs6733379
PheGenIrs6733379
hapmaprs6733379
1000 genomesrs6733379
hgdprs6733379
ensemblrs6733379
gopubmedrs6733379
geneviewrs6733379
scholarrs6733379
googlers6733379
pharmgkbrs6733379
gwascentralrs6733379
openSNPrs6733379
23andMers6733379
23andMe allrs6733379
SNP Nexus

SNPshotrs6733379
SNPdbers6733379
MSV3drs6733379
GWAS Ctlgrs6733379
GMAF0.2259
Max Magnitude
? (G;G) (G;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 G
P-val 0.000004
Odds Ratio NR NR



GET Evidence
rs6733379
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.726562
summary