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rs5016282

From SNPedia

Orientationplus
Stabilizedplus
Make rs5016282(A;A)
Make rs5016282(A;G)
Make rs5016282(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position89008492
GeneGRM5
is asnp
is mentioned by
dbSNPrs5016282
ebirs5016282
HLIrs5016282
Exacrs5016282
Varsomers5016282
Maprs5016282
PheGenIrs5016282
hapmaprs5016282
1000 genomesrs5016282
hgdprs5016282
ensemblrs5016282
gopubmedrs5016282
geneviewrs5016282
scholarrs5016282
googlers5016282
pharmgkbrs5016282
gwascentralrs5016282
openSNPrs5016282
23andMers5016282
23andMe allrs5016282
SNP Nexus

SNPshotrs5016282
SNPdbers5016282
MSV3drs5016282
GWAS Ctlgrs5016282
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22012869]
Trait
Title Genome-wide association study in German patients with attention deficit/hyperactivity disorder.
Risk Allele A
P-val 0.000001
Odds Ratio None None