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rs5941160

From SNPedia

Orientationplus
Stabilizedplus
Make rs5941160(G;G)
Make rs5941160(G;T)
Make rs5941160(T;T)
ReferenceGRCh37.p5 37.3/137
ChromosomeX
Position88530065
is asnp
is mentioned by
dbSNPrs5941160
ebirs5941160
HLIrs5941160
Exacrs5941160
Varsomers5941160
Maprs5941160
PheGenIrs5941160
hapmaprs5941160
1000 genomesrs5941160
hgdprs5941160
ensemblrs5941160
gopubmedrs5941160
geneviewrs5941160
scholarrs5941160
googlers5941160
pharmgkbrs5941160
gwascentralrs5941160
openSNPrs5941160
23andMers5941160
23andMe allrs5941160
SNP Nexus

SNPshotrs5941160
SNPdbers5941160
MSV3drs5941160
GWAS Ctlgrs5941160
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 22808956OA-icon.png]
Trait Antineutrophil cytoplasmic antibody-associated vasculitis
Title Genetically distinct subsets within ANCA-associated vasculitis.
Risk Allele
P-val 2E-20
Odds Ratio NR NR