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rs17057678

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 normal
Make rs17057678(C;C)
Make rs17057678(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position129710348
GeneARHGAP18
is asnp
is mentioned by
dbSNPrs17057678
dbSNP (old)rs17057678
ClinGenrs17057678
ebirs17057678
HLIrs17057678
Exacrs17057678
Gnomadrs17057678
Varsomers17057678
Maprs17057678
PheGenIrs17057678
Biobankrs17057678
1000 genomesrs17057678
hgdprs17057678
ensemblrs17057678
gopubmedrs17057678
geneviewrs17057678
scholarrs17057678
googlers17057678
pharmgkbrs17057678
gwascentralrs17057678
openSNPrs17057678
23andMers17057678
23andMe allrs17057678
SNP Nexus

SNPshotrs17057678
SNPdbers17057678
MSV3drs17057678
GWAS Ctlgrs17057678
GMAF0.09091
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 6E-7
Odds Ratio 1.25 [NR]