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rs6618677

From SNPedia

Orientationplus
Stabilizedplus
Make rs6618677(A;A)
Make rs6618677(A;G)
Make rs6618677(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position91557719
is asnp
is mentioned by
dbSNPrs6618677
ebirs6618677
HLIrs6618677
Exacrs6618677
Varsomers6618677
Maprs6618677
PheGenIrs6618677
hapmaprs6618677
1000 genomesrs6618677
hgdprs6618677
ensemblrs6618677
gopubmedrs6618677
geneviewrs6618677
scholarrs6618677
googlers6618677
pharmgkbrs6618677
gwascentralrs6618677
openSNPrs6618677
23andMers6618677
23andMe allrs6618677
SNP Nexus

SNPshotrs6618677
SNPdbers6618677
MSV3drs6618677
GWAS Ctlgrs6618677
GMAF0.2388
Max Magnitude
? (A;A) (A;G) (G;G) 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 4E-8
Odds Ratio 1.43 [NR]