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rs7227892

From SNPedia

Orientationplus
Stabilizedplus
Make rs7227892(A;A)
Make rs7227892(A;T)
Make rs7227892(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position48810331
GeneCTIF
is asnp
is mentioned by
dbSNPrs7227892
dbSNP (classic)rs7227892
ClinGenrs7227892
ebirs7227892
HLIrs7227892
Exacrs7227892
Gnomadrs7227892
Varsomers7227892
LitVarrs7227892
Maprs7227892
PheGenIrs7227892
Biobankrs7227892
1000 genomesrs7227892
hgdprs7227892
ensemblrs7227892
geneviewrs7227892
scholarrs7227892
googlers7227892
pharmgkbrs7227892
gwascentralrs7227892
openSNPrs7227892
23andMers7227892
SNPshotrs7227892
SNPdbers7227892
MSV3drs7227892
GWAS Ctlgrs7227892
GMAF0.2938
Max Magnitude0
? (A;A) (A;T) (T;T) 28


GWAS snp
PMID [PMID 23793025OA-icon.png]
Trait Migraine with 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]