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rs4392363

From SNPedia

Orientationplus
Stabilizedplus
Make rs4392363(A;A)
Make rs4392363(A;T)
Make rs4392363(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position67093414
is asnp
is mentioned by
dbSNPrs4392363
dbSNP (classic)rs4392363
ClinGenrs4392363
ebirs4392363
HLIrs4392363
Exacrs4392363
Gnomadrs4392363
Varsomers4392363
LitVarrs4392363
Maprs4392363
PheGenIrs4392363
Biobankrs4392363
1000 genomesrs4392363
hgdprs4392363
ensemblrs4392363
geneviewrs4392363
scholarrs4392363
googlers4392363
pharmgkbrs4392363
gwascentralrs4392363
openSNPrs4392363
23andMers4392363
SNPshotrs4392363
SNPdbers4392363
MSV3drs4392363
GWAS Ctlgrs4392363
GMAF0.3673
Max Magnitude0
? (A;A) (A;T) (T;T) 28


GWAS snp
PMID [PMID 23793025OA-icon.png]
Trait Migraine - clinic-based
Title Genome-wide meta-analysis identifies new susceptibility loci for migraine.
Risk Allele
P-val 1E-6
Odds Ratio 1.15 [1.09-1.22]