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rs7900239

From SNPedia

Orientationplus
Stabilizedplus
Make rs7900239(A;A)
Make rs7900239(A;G)
Make rs7900239(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position78755324
is asnp
is mentioned by
dbSNPrs7900239
dbSNP (classic)rs7900239
ClinGenrs7900239
ebirs7900239
HLIrs7900239
Exacrs7900239
Gnomadrs7900239
Varsomers7900239
LitVarrs7900239
Maprs7900239
PheGenIrs7900239
Biobankrs7900239
1000 genomesrs7900239
hgdprs7900239
ensemblrs7900239
geneviewrs7900239
scholarrs7900239
googlers7900239
pharmgkbrs7900239
gwascentralrs7900239
openSNPrs7900239
23andMers7900239
SNPshotrs7900239
SNPdbers7900239
MSV3drs7900239
GWAS Ctlgrs7900239
GMAF0.1947
Max Magnitude0
? (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 A
P-val 9E-6
Odds Ratio 1.09 [1.05-1.13]