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rs4493873

From SNPedia

Orientationplus
Stabilizedplus
Make rs4493873(A;A)
Make rs4493873(A;C)
Make rs4493873(C;C)
ReferenceGRCh38 38.1/141
Chromosome8
Position91063415
GeneLOC100506365
is asnp
is mentioned by
dbSNPrs4493873
ebirs4493873
HLIrs4493873
Exacrs4493873
Varsomers4493873
Maprs4493873
PheGenIrs4493873
hapmaprs4493873
1000 genomesrs4493873
hgdprs4493873
ensemblrs4493873
gopubmedrs4493873
geneviewrs4493873
scholarrs4493873
googlers4493873
pharmgkbrs4493873
gwascentralrs4493873
openSNPrs4493873
23andMers4493873
23andMe allrs4493873
SNP Nexus

SNPshotrs4493873
SNPdbers4493873
MSV3drs4493873
GWAS Ctlgrs4493873
GMAF0.3889
Max Magnitude
? (A;A) (A;C) (C;C) 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 5E-6
Odds Ratio 1.14 [1.08-1.2]