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rs11189853

From SNPedia

Orientationplus
Stabilizedplus
Make rs11189853(A;A)
Make rs11189853(A;G)
Make rs11189853(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position98886424
GeneHPSE2
is asnp
is mentioned by
dbSNPrs11189853
dbSNP (classic)rs11189853
ClinGenrs11189853
ebirs11189853
HLIrs11189853
Exacrs11189853
Gnomadrs11189853
Varsomers11189853
LitVarrs11189853
Maprs11189853
PheGenIrs11189853
Biobankrs11189853
1000 genomesrs11189853
hgdprs11189853
ensemblrs11189853
geneviewrs11189853
scholarrs11189853
googlers11189853
pharmgkbrs11189853
gwascentralrs11189853
openSNPrs11189853
23andMers11189853
SNPshotrs11189853
SNPdbers11189853
MSV3drs11189853
GWAS Ctlgrs11189853
GMAF0.09366
Max Magnitude0
? (A;A) (A;G) (G;G) 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 G
P-val 2E-6
Odds Ratio 1.16 [1.09-1.23]