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rs11134178

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs11134178(C;C)
Make rs11134178(C;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position6834054
is asnp
is mentioned by
dbSNPrs11134178
dbSNP (classic)rs11134178
ClinGenrs11134178
ebirs11134178
HLIrs11134178
Exacrs11134178
Gnomadrs11134178
Varsomers11134178
LitVarrs11134178
Maprs11134178
PheGenIrs11134178
Biobankrs11134178
1000 genomesrs11134178
hgdprs11134178
ensemblrs11134178
geneviewrs11134178
scholarrs11134178
googlers11134178
pharmgkbrs11134178
gwascentralrs11134178
openSNPrs11134178
23andMers11134178
SNPshotrs11134178
SNPdbers11134178
MSV3drs11134178
GWAS Ctlgrs11134178
GMAF0.02296
Max Magnitude0
? (C;C) (C;T) (T;T) 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 T
P-val 0.0000030000000000000001
Odds Ratio NR NR