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rs7718446

From SNPedia

Orientationplus
Stabilizedplus
Make rs7718446(A;A)
Make rs7718446(A;G)
Make rs7718446(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position146369972
is asnp
is mentioned by
dbSNPrs7718446
dbSNP (classic)rs7718446
ClinGenrs7718446
ebirs7718446
HLIrs7718446
Exacrs7718446
Gnomadrs7718446
Varsomers7718446
LitVarrs7718446
Maprs7718446
PheGenIrs7718446
Biobankrs7718446
1000 genomesrs7718446
hgdprs7718446
ensemblrs7718446
geneviewrs7718446
scholarrs7718446
googlers7718446
pharmgkbrs7718446
gwascentralrs7718446
openSNPrs7718446
23andMers7718446
SNPshotrs7718446
SNPdbers7718446
MSV3drs7718446
GWAS Ctlgrs7718446
GMAF0.4353
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
P-val 4E-6
Odds Ratio 1.11 [1.06-1.16]