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rs2986961

From SNPedia

Orientationplus
Stabilizedplus
Make rs2986961(C;C)
Make rs2986961(C;T)
Make rs2986961(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position29798430
is asnp
is mentioned by
dbSNPrs2986961
ebirs2986961
HLIrs2986961
Exacrs2986961
Varsomers2986961
Maprs2986961
PheGenIrs2986961
hapmaprs2986961
1000 genomesrs2986961
hgdprs2986961
ensemblrs2986961
gopubmedrs2986961
geneviewrs2986961
scholarrs2986961
googlers2986961
pharmgkbrs2986961
gwascentralrs2986961
openSNPrs2986961
23andMers2986961
23andMe allrs2986961
SNP Nexus

SNPshotrs2986961
SNPdbers2986961
MSV3drs2986961
GWAS Ctlgrs2986961
GMAF0.3604
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23793025OA-icon.png]
Trait Migraine with aura
Title Genome-wide meta-analysis identifies new susceptibility loci for migraine.
Risk Allele C
P-val 5E-7
Odds Ratio 1.14 [1.08-1.20]