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rs9399032

From SNPedia

Orientationplus
Stabilizedplus
Make rs9399032(A;A)
Make rs9399032(A;T)
Make rs9399032(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position132567800
is asnp
is mentioned by
dbSNPrs9399032
ebirs9399032
HLIrs9399032
Exacrs9399032
Varsomers9399032
Maprs9399032
PheGenIrs9399032
hapmaprs9399032
1000 genomesrs9399032
hgdprs9399032
ensemblrs9399032
gopubmedrs9399032
geneviewrs9399032
scholarrs9399032
googlers9399032
pharmgkbrs9399032
gwascentralrs9399032
openSNPrs9399032
23andMers9399032
23andMe allrs9399032
SNP Nexus

SNPshotrs9399032
SNPdbers9399032
MSV3drs9399032
GWAS Ctlgrs9399032
GMAF0.4752
Max Magnitude
? (A;A) (A;T) (T;T) 28
GWAS snp
PMID [PMID 23793025OA-icon.png]
Trait Migraine without aura
Title Genome-wide meta-analysis identifies new susceptibility loci for migraine.
Risk Allele A
P-val 4E-6
Odds Ratio 1.10 [1.06-1.15]