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rs3790455

From SNPedia

Orientationplus
Stabilizedplus
Make rs3790455(C;C)
Make rs3790455(C;T)
Make rs3790455(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position156486509
GeneMEF2D
is asnp
is mentioned by
dbSNPrs3790455
ebirs3790455
HLIrs3790455
Exacrs3790455
Varsomers3790455
Maprs3790455
PheGenIrs3790455
hapmaprs3790455
1000 genomesrs3790455
hgdprs3790455
ensemblrs3790455
gopubmedrs3790455
geneviewrs3790455
scholarrs3790455
googlers3790455
pharmgkbrs3790455
gwascentralrs3790455
openSNPrs3790455
23andMers3790455
23andMe allrs3790455
SNP Nexus

SNPshotrs3790455
SNPdbers3790455
MSV3drs3790455
GWAS Ctlgrs3790455
GMAF0.4307
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22683712OA-icon.png]
Trait
Title Genome-wide association analysis identifies susceptibility loci for migraine without aura.
Risk Allele C
P-val 7E-11
Odds Ratio 1.2000 None


[PMID 24674449OA-icon.png] A replication study of GWAS findings in migraine identifies association in a Swedish case-control sample