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rs2186141

From SNPedia

Orientationminus
Stabilizedminus
Make rs2186141(A;A)
Make rs2186141(A;G)
Make rs2186141(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position153683836
is asnp
is mentioned by
dbSNPrs2186141
ebirs2186141
HLIrs2186141
Exacrs2186141
Varsomers2186141
Maprs2186141
PheGenIrs2186141
hapmaprs2186141
1000 genomesrs2186141
hgdprs2186141
ensemblrs2186141
gopubmedrs2186141
geneviewrs2186141
scholarrs2186141
googlers2186141
pharmgkbrs2186141
gwascentralrs2186141
openSNPrs2186141
23andMers2186141
23andMe allrs2186141
SNP Nexus

SNPshotrs2186141
SNPdbers2186141
MSV3drs2186141
GWAS Ctlgrs2186141
GMAF0.4339
Max Magnitude
? (A;A) (A;G) (G;G) 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 4E-6
Odds Ratio 1.12 [1.06-1.18]