rs11724635

Orientation

plus

Stabilized

plus

Make rs11724635(A;A)

Make rs11724635(A;C)

Make rs11724635(C;C)

Reference

GRCh38 38.1/141

Chromosome

4

Position

15735478

Gene

BST1

is a	snp
is	mentioned by
dbSNP	rs11724635
dbSNP (classic)	rs11724635
ClinGen	rs11724635
ebi	rs11724635
HLI	rs11724635
Exac	rs11724635
Gnomad	rs11724635
Varsome	rs11724635
LitVar	rs11724635
Map	rs11724635
PheGenI	rs11724635
Biobank	rs11724635
1000 genomes	rs11724635
hgdp	rs11724635
ensembl	rs11724635
geneview	rs11724635
scholar	rs11724635
google	rs11724635
pharmgkb	rs11724635
gwascentral	rs11724635
openSNP	rs11724635
23andMe	rs11724635
SNPshot	rs11724635
SNPdbe	rs11724635
MSV3d	rs11724635
GWAS Ctlg	rs11724635

GMAF

0.4036

Max Magnitude

0

?	(A;A) (A;C) (C;C)	28

GWAS snp
PMID	[PMID 21292315]
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 22786590] 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