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rs1515641

From SNPedia

Orientationplus
Stabilizedplus
Make rs1515641(A;A)
Make rs1515641(A;G)
Make rs1515641(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position127803924
GeneCCDC192
is asnp
is mentioned by
dbSNPrs1515641
dbSNP (classic)rs1515641
ClinGenrs1515641
ebirs1515641
HLIrs1515641
Exacrs1515641
Gnomadrs1515641
Varsomers1515641
LitVarrs1515641
Maprs1515641
PheGenIrs1515641
Biobankrs1515641
1000 genomesrs1515641
hgdprs1515641
ensemblrs1515641
geneviewrs1515641
scholarrs1515641
googlers1515641
pharmgkbrs1515641
gwascentralrs1515641
openSNPrs1515641
23andMers1515641
SNPshotrs1515641
SNPdbers1515641
MSV3drs1515641
GWAS Ctlgrs1515641
GMAF0.1056
Max Magnitude0
? (A;A) (A;G) (G;G) 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 4E-6
Odds Ratio NR NR


[PMID 17903302OA-icon.png] Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.