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rs6998277

From SNPedia

Orientationplus
Stabilizedplus
Make rs6998277(C;C)
Make rs6998277(C;T)
Make rs6998277(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position102627713
is asnp
is mentioned by
dbSNPrs6998277
ebirs6998277
HLIrs6998277
Exacrs6998277
Varsomers6998277
Maprs6998277
PheGenIrs6998277
hapmaprs6998277
1000 genomesrs6998277
hgdprs6998277
ensemblrs6998277
gopubmedrs6998277
geneviewrs6998277
scholarrs6998277
googlers6998277
pharmgkbrs6998277
gwascentralrs6998277
openSNPrs6998277
23andMers6998277
23andMe allrs6998277
SNP Nexus

SNPshotrs6998277
SNPdbers6998277
MSV3drs6998277
GWAS Ctlgrs6998277
GMAF0.236
Max Magnitude
? (C;C) (C;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 C
P-val 2E-6
Odds Ratio 1.07 [1.04-1.10]