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rs4738393

From SNPedia

Orientationplus
Stabilizedplus
Make rs4738393(A;A)
Make rs4738393(A;G)
Make rs4738393(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position55687218
is asnp
is mentioned by
dbSNPrs4738393
dbSNP (classic)rs4738393
ClinGenrs4738393
ebirs4738393
HLIrs4738393
Exacrs4738393
Gnomadrs4738393
Varsomers4738393
LitVarrs4738393
Maprs4738393
PheGenIrs4738393
Biobankrs4738393
1000 genomesrs4738393
hgdprs4738393
ensemblrs4738393
geneviewrs4738393
scholarrs4738393
googlers4738393
pharmgkbrs4738393
gwascentralrs4738393
openSNPrs4738393
23andMers4738393
SNPshotrs4738393
SNPdbers4738393
MSV3drs4738393
GWAS Ctlgrs4738393
GMAF0.3595
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 23793025OA-icon.png]
Trait Migraine - clinic-based
Title Genome-wide meta-analysis identifies new susceptibility loci for migraine.
Risk Allele
P-val 6E-6
Odds Ratio 1.09 [1.09-1.22]