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rs16904191

From SNPedia

Orientationplus
Stabilizedplus
Make rs16904191(A;A)
Make rs16904191(A;G)
Make rs16904191(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position130021250
is asnp
is mentioned by
dbSNPrs16904191
ebirs16904191
HLIrs16904191
Exacrs16904191
Varsomers16904191
Maprs16904191
PheGenIrs16904191
hapmaprs16904191
1000 genomesrs16904191
hgdprs16904191
ensemblrs16904191
gopubmedrs16904191
geneviewrs16904191
scholarrs16904191
googlers16904191
pharmgkbrs16904191
gwascentralrs16904191
openSNPrs16904191
23andMers16904191
23andMe allrs16904191
SNP Nexus

SNPshotrs16904191
SNPdbers16904191
MSV3drs16904191
GWAS Ctlgrs16904191
GMAF0.4463
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 G
P-val 2E-7
Odds Ratio 1.07 [1.04-1.09]