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rs705162

From SNPedia

Orientationplus
Stabilizedplus
Make rs705162(A;A)
Make rs705162(A;G)
Make rs705162(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position123492159
is asnp
is mentioned by
dbSNPrs705162
ebirs705162
HLIrs705162
Exacrs705162
Varsomers705162
Maprs705162
PheGenIrs705162
hapmaprs705162
1000 genomesrs705162
hgdprs705162
ensemblrs705162
gopubmedrs705162
geneviewrs705162
scholarrs705162
googlers705162
pharmgkbrs705162
gwascentralrs705162
openSNPrs705162
23andMers705162
23andMe allrs705162
SNP Nexus

SNPshotrs705162
SNPdbers705162
MSV3drs705162
GWAS Ctlgrs705162
GMAF0.236
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 A
P-val 3E-6
Odds Ratio 1.06 [1.04-1.09]