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rs1521882

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs1521882(C;C)
Make rs1521882(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position202085128
GeneLOC100505748
is asnp
is mentioned by
dbSNPrs1521882
ebirs1521882
HLIrs1521882
Exacrs1521882
Varsomers1521882
Maprs1521882
PheGenIrs1521882
hapmaprs1521882
1000 genomesrs1521882
hgdprs1521882
ensemblrs1521882
gopubmedrs1521882
geneviewrs1521882
scholarrs1521882
googlers1521882
pharmgkbrs1521882
gwascentralrs1521882
openSNPrs1521882
23andMers1521882
23andMe allrs1521882
SNP Nexus

SNPshotrs1521882
SNPdbers1521882
MSV3drs1521882
GWAS Ctlgrs1521882
GMAF0.2025
Max Magnitude0
? (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 A
P-val 0.000008
Odds Ratio NR NR



GET Evidence
rs1521882
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.75
summary