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rs10463832

From SNPedia

Orientationplus
Stabilizedplus
Make rs10463832(A;A)
Make rs10463832(A;C)
Make rs10463832(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position127774794
GeneCCDC192
is asnp
is mentioned by
dbSNPrs10463832
dbSNP (old)rs10463832
ClinGenrs10463832
ebirs10463832
HLIrs10463832
Exacrs10463832
Gnomadrs10463832
Varsomers10463832
Maprs10463832
PheGenIrs10463832
Biobankrs10463832
1000 genomesrs10463832
hgdprs10463832
ensemblrs10463832
gopubmedrs10463832
geneviewrs10463832
scholarrs10463832
googlers10463832
pharmgkbrs10463832
gwascentralrs10463832
openSNPrs10463832
23andMers10463832
23andMe allrs10463832
SNP Nexus

SNPshotrs10463832
SNPdbers10463832
MSV3drs10463832
GWAS Ctlgrs10463832
GMAF0.1038
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23527680]
Trait Attention deficit hyperactivity disorder (hyperactivity-impulsivity symptoms)
Title Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits.
Risk Allele A
P-val 5E-6
Odds Ratio NR NR