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rs6983777

From SNPedia

Orientationplus
Stabilizedplus
Make rs6983777(A;A)
Make rs6983777(A;G)
Make rs6983777(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position103106338
is asnp
is mentioned by
dbSNPrs6983777
ebirs6983777
HLIrs6983777
Exacrs6983777
Varsomers6983777
Maprs6983777
PheGenIrs6983777
hapmaprs6983777
1000 genomesrs6983777
hgdprs6983777
ensemblrs6983777
gopubmedrs6983777
geneviewrs6983777
scholarrs6983777
googlers6983777
pharmgkbrs6983777
gwascentralrs6983777
openSNPrs6983777
23andMers6983777
23andMe allrs6983777
SNP Nexus

SNPshotrs6983777
SNPdbers6983777
MSV3drs6983777
GWAS Ctlgrs6983777
GMAF0.4798
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23527680]
Trait Attention deficit hyperactivity disorder (combined symptoms)
Title Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits.
Risk Allele A
P-val 8E-6
Odds Ratio NR NR