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rs12006166

From SNPedia

Orientationplus
Stabilizedplus
Make rs12006166(A;A)
Make rs12006166(A;T)
Make rs12006166(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position115662708
is asnp
is mentioned by
dbSNPrs12006166
ebirs12006166
HLIrs12006166
Exacrs12006166
Varsomers12006166
Maprs12006166
PheGenIrs12006166
hapmaprs12006166
1000 genomesrs12006166
hgdprs12006166
ensemblrs12006166
gopubmedrs12006166
geneviewrs12006166
scholarrs12006166
googlers12006166
pharmgkbrs12006166
gwascentralrs12006166
openSNPrs12006166
23andMers12006166
23andMe allrs12006166
SNP Nexus

SNPshotrs12006166
SNPdbers12006166
MSV3drs12006166
GWAS Ctlgrs12006166
GMAF0.09091
Max Magnitude
? (A;A) (A;T) (T;T) 28
GWAS snp
PMID [PMID 23793025OA-icon.png]
Trait Migraine
Title Genome-wide meta-analysis identifies new susceptibility loci for migraine.
Risk Allele T
P-val 9E-7
Odds Ratio 1.08 [1.05-1.12]