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rs2078371

From SNPedia

Orientationplus
Stabilizedplus
Make rs2078371(C;C)
Make rs2078371(C;T)
Make rs2078371(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position115134562
is asnp
is mentioned by
dbSNPrs2078371
dbSNP (old)rs2078371
ClinGenrs2078371
ebirs2078371
HLIrs2078371
Exacrs2078371
Gnomadrs2078371
Varsomers2078371
Maprs2078371
PheGenIrs2078371
Biobankrs2078371
1000 genomesrs2078371
hgdprs2078371
ensemblrs2078371
gopubmedrs2078371
geneviewrs2078371
scholarrs2078371
googlers2078371
pharmgkbrs2078371
gwascentralrs2078371
openSNPrs2078371
23andMers2078371
23andMe allrs2078371
SNP Nexus

SNPshotrs2078371
SNPdbers2078371
MSV3drs2078371
GWAS Ctlgrs2078371
GMAF0.1267
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 23294458] Replication and meta-analysis of common variants identifies a genome-wide significant locus in migraine