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rs11594111

From SNPedia

Orientationplus
Stabilizedplus
Make rs11594111(A;A)
Make rs11594111(A;G)
Make rs11594111(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position14903407
GeneSUV39H2
is asnp
is mentioned by
dbSNPrs11594111
ebirs11594111
HLIrs11594111
Exacrs11594111
Varsomers11594111
Maprs11594111
PheGenIrs11594111
hapmaprs11594111
1000 genomesrs11594111
hgdprs11594111
ensemblrs11594111
gopubmedrs11594111
geneviewrs11594111
scholarrs11594111
googlers11594111
pharmgkbrs11594111
gwascentralrs11594111
openSNPrs11594111
23andMers11594111
23andMe allrs11594111
SNP Nexus

SNPshotrs11594111
SNPdbers11594111
MSV3drs11594111
GWAS Ctlgrs11594111
GMAF0.06566
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23793025OA-icon.png]
Trait Migraine
Title Genome-wide meta-analysis identifies new susceptibility loci for migraine.
Risk Allele G
P-val 1E-7
Odds Ratio 1.09 [1.06-1.12]