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rs4759042

From SNPedia

Orientationplus
Stabilizedplus
Make rs4759042(C;C)
Make rs4759042(C;T)
Make rs4759042(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position56983563
GeneUGT2B24P
is asnp
is mentioned by
dbSNPrs4759042
ebirs4759042
HLIrs4759042
Exacrs4759042
Varsomers4759042
Maprs4759042
PheGenIrs4759042
hapmaprs4759042
1000 genomesrs4759042
hgdprs4759042
ensemblrs4759042
gopubmedrs4759042
geneviewrs4759042
scholarrs4759042
googlers4759042
pharmgkbrs4759042
gwascentralrs4759042
openSNPrs4759042
23andMers4759042
23andMe allrs4759042
SNP Nexus

SNPshotrs4759042
SNPdbers4759042
MSV3drs4759042
GWAS Ctlgrs4759042
GMAF0.2328
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23793025OA-icon.png]
Trait Migraine
Title Genome-wide meta-analysis identifies new susceptibility loci for migraine.
Risk Allele
P-val 3E-6
Odds Ratio 1.05 [1.03-1.09]