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rs11158026

From SNPedia
Orientationplus
Stabilizedplus
Make rs11158026(C;C)
Make rs11158026(C;T)
Make rs11158026(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome14
Position54882151
GeneGCH1
is asnp
is mentioned by
dbSNPrs11158026
dbSNP (old)rs11158026
ClinGenrs11158026
ebirs11158026
HLIrs11158026
Exacrs11158026
Gnomadrs11158026
Varsomers11158026
Maprs11158026
PheGenIrs11158026
Biobankrs11158026
1000 genomesrs11158026
hgdprs11158026
ensemblrs11158026
gopubmedrs11158026
geneviewrs11158026
scholarrs11158026
googlers11158026
pharmgkbrs11158026
gwascentralrs11158026
openSNPrs11158026
23andMers11158026
23andMe allrs11158026
SNPshotrs11158026
SNPdbers11158026
MSV3drs11158026
GWAS Ctlgrs11158026
Max Magnitude
rs11158026(T) allele carriers show a slight increase in risk for Parkinson's disease, based on a study of ~200 patients; odds ratio 1.23, p = 0.048 (i.e. on the border of being considered statistically non-significant).[PMID 27871051]