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rs11724635

From SNPedia

Orientationplus
Stabilizedplus
Make rs11724635(A;A)
Make rs11724635(A;C)
Make rs11724635(C;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position15735478
GeneBST1
is asnp
is mentioned by
dbSNPrs11724635
ebirs11724635
HLIrs11724635
Exacrs11724635
Varsomers11724635
Maprs11724635
PheGenIrs11724635
hapmaprs11724635
1000 genomesrs11724635
hgdprs11724635
ensemblrs11724635
gopubmedrs11724635
geneviewrs11724635
scholarrs11724635
googlers11724635
pharmgkbrs11724635
gwascentralrs11724635
openSNPrs11724635
23andMers11724635
23andMe allrs11724635
SNP Nexus

SNPshotrs11724635
SNPdbers11724635
MSV3drs11724635
GWAS Ctlgrs11724635
GMAF0.4036
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 21292315OA-icon.png]
Trait
Title Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
Risk Allele A
P-val 1E-16
Odds Ratio 1.1500 [1.11-1.19]

[PMID 23026536] Lack of association between BST1 polymorphisms and sporadic Parkinson's disease in a Japanese population

[PMID 22786590OA-icon.png] Large-scale replication and heterogeneity in Parkinson disease genetic loci

[PMID 23853107] Analysis of genome-wide association study-linked loci in Parkinson's disease of Mainland China

[PMID 24342025] BST1 rs11724635 interacts with environmental factors to increase the risk of Parkinson's disease in a Taiwanese population