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rs10849061

From SNPedia

Orientationplus
Stabilizedplus
Make rs10849061(C;C)
Make rs10849061(C;T)
Make rs10849061(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position4414290
is asnp
is mentioned by
dbSNPrs10849061
dbSNP (classic)rs10849061
ClinGenrs10849061
ebirs10849061
HLIrs10849061
Exacrs10849061
Gnomadrs10849061
Varsomers10849061
LitVarrs10849061
Maprs10849061
PheGenIrs10849061
Biobankrs10849061
1000 genomesrs10849061
hgdprs10849061
ensemblrs10849061
geneviewrs10849061
scholarrs10849061
googlers10849061
pharmgkbrs10849061
gwascentralrs10849061
openSNPrs10849061
23andMers10849061
SNPshotrs10849061
SNPdbers10849061
MSV3drs10849061
GWAS Ctlgrs10849061
GMAF0.3999
Max Magnitude0
? (C;C) (C;T) (T;T) 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 2E-7
Odds Ratio 1.06 [1.04-1.09]