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

rs9947662

From SNPedia

Orientationplus
Stabilizedplus
Make rs9947662(A;A)
Make rs9947662(A;G)
Make rs9947662(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position47333893
is asnp
is mentioned by
dbSNPrs9947662
ebirs9947662
HLIrs9947662
Exacrs9947662
Varsomers9947662
Maprs9947662
PheGenIrs9947662
hapmaprs9947662
1000 genomesrs9947662
hgdprs9947662
ensemblrs9947662
gopubmedrs9947662
geneviewrs9947662
scholarrs9947662
googlers9947662
pharmgkbrs9947662
gwascentralrs9947662
openSNPrs9947662
23andMers9947662
23andMe allrs9947662
SNP Nexus

SNPshotrs9947662
SNPdbers9947662
MSV3drs9947662
GWAS Ctlgrs9947662
GMAF0.2406
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23793025OA-icon.png]
Trait Migraine
Title Genome-wide meta-analysis identifies new susceptibility loci for migraine.
Risk Allele
P-val 3E-6
Odds Ratio 1.06 [1.03-1.09]