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rs11696973

From SNPedia

Orientationplus
Stabilizedplus
Make rs11696973(G;G)
Make rs11696973(G;T)
Make rs11696973(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position55551451
is asnp
is mentioned by
dbSNPrs11696973
ebirs11696973
HLIrs11696973
Exacrs11696973
Varsomers11696973
Maprs11696973
PheGenIrs11696973
hapmaprs11696973
1000 genomesrs11696973
hgdprs11696973
ensemblrs11696973
gopubmedrs11696973
geneviewrs11696973
scholarrs11696973
googlers11696973
pharmgkbrs11696973
gwascentralrs11696973
openSNPrs11696973
23andMers11696973
23andMe allrs11696973
SNP Nexus

SNPshotrs11696973
SNPdbers11696973
MSV3drs11696973
GWAS Ctlgrs11696973
GMAF0.1028
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 23793025OA-icon.png]
Trait Migraine without aura
Title Genome-wide meta-analysis identifies new susceptibility loci for migraine.
Risk Allele
P-val 8E-6
Odds Ratio 1.15 [1.09-1.22]