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rs12282928

From SNPedia

Orientationplus
Stabilizedplus
Make rs12282928(A;A)
Make rs12282928(A;G)
Make rs12282928(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position48310476
is asnp
is mentioned by
dbSNPrs12282928
ebirs12282928
HLIrs12282928
Exacrs12282928
Varsomers12282928
Maprs12282928
PheGenIrs12282928
hapmaprs12282928
1000 genomesrs12282928
hgdprs12282928
ensemblrs12282928
gopubmedrs12282928
geneviewrs12282928
scholarrs12282928
googlers12282928
pharmgkbrs12282928
gwascentralrs12282928
openSNPrs12282928
23andMers12282928
23andMe allrs12282928
SNP Nexus

SNPshotrs12282928
SNPdbers12282928
MSV3drs12282928
GWAS Ctlgrs12282928
GMAF0.3398
Max Magnitude
? (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 9E-6
Odds Ratio 1.14 [1.08-1.2]