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rs1861960

From SNPedia

Orientationplus
Stabilizedplus
Make rs1861960(G;G)
Make rs1861960(G;T)
Make rs1861960(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position155492440
is asnp
is mentioned by
dbSNPrs1861960
ebirs1861960
HLIrs1861960
Exacrs1861960
Varsomers1861960
Maprs1861960
PheGenIrs1861960
hapmaprs1861960
1000 genomesrs1861960
hgdprs1861960
ensemblrs1861960
gopubmedrs1861960
geneviewrs1861960
scholarrs1861960
googlers1861960
pharmgkbrs1861960
gwascentralrs1861960
openSNPrs1861960
23andMers1861960
23andMe allrs1861960
SNP Nexus

SNPshotrs1861960
SNPdbers1861960
MSV3drs1861960
GWAS Ctlgrs1861960
GMAF0.3641
Max Magnitude
? (G;G) (G;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 T
P-val 6E-6
Odds Ratio 1.07 [1.04-1.10]