Have questions? Visit https://www.reddit.com/r/SNPedia

rs2074193

From SNPedia

Orientationplus
Stabilizedplus
Make rs2074193(G;G)
Make rs2074193(G;T)
Make rs2074193(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position47377646
is asnp
is mentioned by
dbSNPrs2074193
ebirs2074193
HLIrs2074193
Exacrs2074193
Varsomers2074193
Maprs2074193
PheGenIrs2074193
hapmaprs2074193
1000 genomesrs2074193
hgdprs2074193
ensemblrs2074193
gopubmedrs2074193
geneviewrs2074193
scholarrs2074193
googlers2074193
pharmgkbrs2074193
gwascentralrs2074193
openSNPrs2074193
23andMers2074193
23andMe allrs2074193
SNP Nexus

SNPshotrs2074193
SNPdbers2074193
MSV3drs2074193
GWAS Ctlgrs2074193
GMAF0.169
Max Magnitude
? (G;G) (G;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 C
P-val 5E-7
Odds Ratio 1.15 [1.09-1.21]