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rs16985493

From SNPedia

Orientationplus
Stabilizedplus
Make rs16985493(A;A)
Make rs16985493(A;G)
Make rs16985493(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position61718507
GeneCDH4
is asnp
is mentioned by
dbSNPrs16985493
dbSNP (classic)rs16985493
ClinGenrs16985493
ebirs16985493
HLIrs16985493
Exacrs16985493
Gnomadrs16985493
Varsomers16985493
LitVarrs16985493
Maprs16985493
PheGenIrs16985493
Biobankrs16985493
1000 genomesrs16985493
hgdprs16985493
ensemblrs16985493
geneviewrs16985493
scholarrs16985493
googlers16985493
pharmgkbrs16985493
gwascentralrs16985493
openSNPrs16985493
23andMers16985493
SNPshotrs16985493
SNPdbers16985493
MSV3drs16985493
GWAS Ctlgrs16985493
GMAF0.04132
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 A
P-val 4E-6
Odds Ratio 1.37 [1.20-1.57]