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rs11906854

From SNPedia

Orientationplus
Stabilizedplus
Make rs11906854(A;A)
Make rs11906854(A;G)
Make rs11906854(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position35795712
GenePHF20
is asnp
is mentioned by
dbSNPrs11906854
dbSNP (classic)rs11906854
ClinGenrs11906854
ebirs11906854
HLIrs11906854
Exacrs11906854
Gnomadrs11906854
Varsomers11906854
LitVarrs11906854
Maprs11906854
PheGenIrs11906854
Biobankrs11906854
1000 genomesrs11906854
hgdprs11906854
ensemblrs11906854
geneviewrs11906854
scholarrs11906854
googlers11906854
pharmgkbrs11906854
gwascentralrs11906854
openSNPrs11906854
23andMers11906854
SNPshotrs11906854
SNPdbers11906854
MSV3drs11906854
GWAS Ctlgrs11906854
GMAF0.1543
Max Magnitude0
? (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 G
P-val 7E-6
Odds Ratio 1.17 [1.09-1.26]