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rs2266886

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) normal
(C;T) 0.26x reduced risk for Meniere's disease
(T;T) 0.26x reduced risk for Meniere's disease
ReferenceGRCh38 38.1/141
ChromosomeX
Position153965901
GeneHCFC1
is asnp
is mentioned by
dbSNPrs2266886
ebirs2266886
HLIrs2266886
Exacrs2266886
Varsomers2266886
Maprs2266886
PheGenIrs2266886
hapmaprs2266886
1000 genomesrs2266886
hgdprs2266886
ensemblrs2266886
gopubmedrs2266886
geneviewrs2266886
scholarrs2266886
googlers2266886
pharmgkbrs2266886
gwascentralrs2266886
openSNPrs2266886
23andMers2266886
23andMe allrs2266886
SNP Nexus

SNPshotrs2266886
SNPdbers2266886
MSV3drs2266886
GWAS Ctlgrs2266886
GMAF0.4988
Max Magnitude
rs2266886 is a SNP in the host cell factor C1 HCFC1 gene, encoding a protein also known as the VP16-accessory protein.

A case-control association study concluded that carriers of a rs2266886(T) minor allele at this SNP have a reduced risk for developing Meniere's disease, by an odds ratio of 0.26 (CI: 0.010-0.65; p = 0.003)[PMID 18520591OA-icon.png]