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rs4704296

From SNPedia

Orientationplus
Stabilizedplus
Make rs4704296(C;C)
Make rs4704296(C;G)
Make rs4704296(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position76206585
GeneSV2C
is asnp
is mentioned by
dbSNPrs4704296
ebirs4704296
HLIrs4704296
Exacrs4704296
Varsomers4704296
Maprs4704296
PheGenIrs4704296
hapmaprs4704296
1000 genomesrs4704296
hgdprs4704296
ensemblrs4704296
gopubmedrs4704296
geneviewrs4704296
scholarrs4704296
googlers4704296
pharmgkbrs4704296
gwascentralrs4704296
openSNPrs4704296
23andMers4704296
23andMe allrs4704296
SNP Nexus

SNPshotrs4704296
SNPdbers4704296
MSV3drs4704296
GWAS Ctlgrs4704296
GMAF0.2971
Max Magnitude
? (C;C) (C;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 1.11 [1.06-1.18]