Have questions? Visit https://www.reddit.com/r/SNPedia

rs9627183

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common on affy axiom data
Make rs9627183(A;A)
Make rs9627183(A;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position47888765
is asnp
is mentioned by
dbSNPrs9627183
ebirs9627183
HLIrs9627183
Exacrs9627183
Varsomers9627183
Maprs9627183
PheGenIrs9627183
hapmaprs9627183
1000 genomesrs9627183
hgdprs9627183
ensemblrs9627183
gopubmedrs9627183
geneviewrs9627183
scholarrs9627183
googlers9627183
pharmgkbrs9627183
gwascentralrs9627183
openSNPrs9627183
23andMers9627183
23andMe allrs9627183
SNP Nexus

SNPshotrs9627183
SNPdbers9627183
MSV3drs9627183
GWAS Ctlgrs9627183
GMAF0.05372
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 18821564]
Trait Attention-deficit/hyperactivity disorder
Title Genome-wide association study of response to methylphenidate in 187 children with attention-deficit/hyperactivity disorder
Risk Allele C
P-val 0.0000030000000000000001
Odds Ratio NR NR

Associated with Attention deficit hyperactivity disorder.




GET Evidence
rs9627183
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.031746
summary