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rs7085387

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G)
(G;G)


Make rs7085387(A;A)
ReferenceGRCh38 38.1/142
Chromosome10
Position58444842
is asnp
is mentioned by
dbSNPrs7085387
ebirs7085387
HLIrs7085387
Exacrs7085387
Varsomers7085387
Maprs7085387
PheGenIrs7085387
hapmaprs7085387
1000 genomesrs7085387
hgdprs7085387
ensemblrs7085387
gopubmedrs7085387
geneviewrs7085387
scholarrs7085387
googlers7085387
pharmgkbrs7085387
gwascentralrs7085387
openSNPrs7085387
23andMers7085387
23andMe allrs7085387
SNP Nexus

SNPshotrs7085387
SNPdbers7085387
MSV3drs7085387
GWAS Ctlgrs7085387
GMAF0.3792
Max Magnitude
? (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
P-val 2E-6
Odds Ratio 1.14 [1.08-1.19]

Rs7085387 is an A/G variant located on chromosome 10 and has been linked to migraines without aura [PMID 23793025OA-icon.png]