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rs577969

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common genotype
Make rs577969(A;A)
Make rs577969(A;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position98531419
GeneHPSE2
is asnp
is mentioned by
dbSNPrs577969
dbSNP (classic)rs577969
ClinGenrs577969
ebirs577969
HLIrs577969
Exacrs577969
Gnomadrs577969
Varsomers577969
LitVarrs577969
Maprs577969
PheGenIrs577969
Biobankrs577969
1000 genomesrs577969
hgdprs577969
ensemblrs577969
geneviewrs577969
scholarrs577969
googlers577969
pharmgkbrs577969
gwascentralrs577969
openSNPrs577969
23andMers577969
SNPshotrs577969
SNPdbers577969
MSV3drs577969
GWAS Ctlgrs577969
GMAF0.03765
Max Magnitude0
? (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 T
P-val 4E-6
Odds Ratio 1.13 [1.07-1.19]