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rs6695352

From SNPedia

Orientationplus
Stabilizedplus
Make rs6695352(C;C)
Make rs6695352(C;T)
Make rs6695352(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position214781596
is asnp
is mentioned by
dbSNPrs6695352
ebirs6695352
HLIrs6695352
Exacrs6695352
Varsomers6695352
Maprs6695352
PheGenIrs6695352
hapmaprs6695352
1000 genomesrs6695352
hgdprs6695352
ensemblrs6695352
gopubmedrs6695352
geneviewrs6695352
scholarrs6695352
googlers6695352
pharmgkbrs6695352
gwascentralrs6695352
openSNPrs6695352
23andMers6695352
23andMe allrs6695352
SNP Nexus

SNPshotrs6695352
SNPdbers6695352
MSV3drs6695352
GWAS Ctlgrs6695352
GMAF0.3999
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23793025OA-icon.png]
Trait Migraine without aura
Title Genome-wide meta-analysis identifies new susceptibility loci for migraine.
Risk Allele
P-val 4E-6
Odds Ratio 1.10 [1.05-1.15]