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rs11816922

From SNPedia

Orientationplus
Stabilizedplus
Make rs11816922(A;A)
Make rs11816922(A;C)
Make rs11816922(C;C)
ReferenceGRCh38 38.1/142
Chromosome10
Position6882482
is asnp
is mentioned by
dbSNPrs11816922
ebirs11816922
HLIrs11816922
Exacrs11816922
Varsomers11816922
Maprs11816922
PheGenIrs11816922
hapmaprs11816922
1000 genomesrs11816922
hgdprs11816922
ensemblrs11816922
gopubmedrs11816922
geneviewrs11816922
scholarrs11816922
googlers11816922
pharmgkbrs11816922
gwascentralrs11816922
openSNPrs11816922
23andMers11816922
23andMe allrs11816922
SNP Nexus

SNPshotrs11816922
SNPdbers11816922
MSV3drs11816922
GWAS Ctlgrs11816922
GMAF0.08999
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23793025OA-icon.png]
Trait Migraine
Title Genome-wide meta-analysis identifies new susceptibility loci for migraine.
Risk Allele A
P-val 5E-6
Odds Ratio 1.10 [1.05-1.14]