Rs10492664

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Orientationminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs10492664(A;A)
Make rs10492664(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position108163877
is asnp
is mentioned by
dbSNPrs10492664
Exacrs10492664
PheGenIrs10492664
nextbiors10492664
hapmaprs10492664
1000 genomesrs10492664
hgdprs10492664
ensemblrs10492664
gopubmedrs10492664
geneviewrs10492664
scholarrs10492664
googlers10492664
pharmgkbrs10492664
gwascentralrs10492664
openSNPrs10492664
23andMers10492664
23andMe allrs10492664
SNP Nexus

SNPshotrs10492664
SNPdbers10492664
MSV3drs10492664
GMAF0.2236
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 C
P-val 0.000001
Odds Ratio NR NR



GET Evidence
rs10492664
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.25
summary