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rs185694

From SNPedia

Orientationminus
Stabilizedminus
Make rs185694(C;C)
Make rs185694(C;T)
Make rs185694(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position30311086
is asnp
is mentioned by
dbSNPrs185694
dbSNP (classic)rs185694
ClinGenrs185694
ebirs185694
HLIrs185694
Exacrs185694
Gnomadrs185694
Varsomers185694
LitVarrs185694
Maprs185694
PheGenIrs185694
Biobankrs185694
1000 genomesrs185694
hgdprs185694
ensemblrs185694
geneviewrs185694
scholarrs185694
googlers185694
pharmgkbrs185694
gwascentralrs185694
openSNPrs185694
23andMers185694
SNPshotrs185694
SNPdbers185694
MSV3drs185694
GWAS Ctlgrs185694
GMAF0.141
Max Magnitude0
? (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 4E-6
Odds Ratio NR NR