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rs4909945

From SNPedia

Orientationplus
Stabilizedplus
Make rs4909945(C;C)
Make rs4909945(C;T)
Make rs4909945(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position10652192
GeneMRVI1
is asnp
is mentioned by
dbSNPrs4909945
ebirs4909945
HLIrs4909945
Exacrs4909945
Varsomers4909945
Maprs4909945
PheGenIrs4909945
hapmaprs4909945
1000 genomesrs4909945
hgdprs4909945
ensemblrs4909945
gopubmedrs4909945
geneviewrs4909945
scholarrs4909945
googlers4909945
pharmgkbrs4909945
gwascentralrs4909945
openSNPrs4909945
23andMers4909945
23andMe allrs4909945
SNP Nexus

SNPshotrs4909945
SNPdbers4909945
MSV3drs4909945
GWAS Ctlgrs4909945
GMAF0.1579
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23793025OA-icon.png]
Trait Migraine
Title Genome-wide meta-analysis identifies new susceptibility loci for migraine.
Risk Allele
P-val 2E-7
Odds Ratio 1.06 [1.04-1.09]