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rs6638512

From SNPedia

Orientationplus
Stabilizedplus
Make rs6638512(C;C)
Make rs6638512(C;T)
Make rs6638512(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position5266661
is asnp
is mentioned by
dbSNPrs6638512
ebirs6638512
HLIrs6638512
Exacrs6638512
Varsomers6638512
Maprs6638512
PheGenIrs6638512
hapmaprs6638512
1000 genomesrs6638512
hgdprs6638512
ensemblrs6638512
gopubmedrs6638512
geneviewrs6638512
scholarrs6638512
googlers6638512
pharmgkbrs6638512
gwascentralrs6638512
openSNPrs6638512
23andMers6638512
23andMe allrs6638512
SNP Nexus

SNPshotrs6638512
SNPdbers6638512
MSV3drs6638512
GWAS Ctlgrs6638512
GMAF0.4299
Max Magnitude
? (C;C) (C;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-25
Odds Ratio NR NR