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rs10180522

From SNPedia

Orientationplus
Stabilizedplus
Make rs10180522(A;A)
Make rs10180522(A;C)
Make rs10180522(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position145314285
is asnp
is mentioned by
dbSNPrs10180522
ebirs10180522
HLIrs10180522
Exacrs10180522
Varsomers10180522
Maprs10180522
PheGenIrs10180522
hapmaprs10180522
1000 genomesrs10180522
hgdprs10180522
ensemblrs10180522
gopubmedrs10180522
geneviewrs10180522
scholarrs10180522
googlers10180522
pharmgkbrs10180522
gwascentralrs10180522
openSNPrs10180522
23andMers10180522
23andMe allrs10180522
SNP Nexus

SNPshotrs10180522
SNPdbers10180522
MSV3drs10180522
GWAS Ctlgrs10180522
GMAF0.2002
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23527680]
Trait Attention deficit hyperactivity disorder (inattention symptoms)
Title Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits.
Risk Allele A
P-val 7E-6
Odds Ratio NR NR