BST1, bone marrow stromal cell antigen 1, 683

N. diseases: 41; N. variants: 14
Disease: Parkinson Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11931532
rs11931532
Entrez Id: 683
Gene Symbol: BST1
BST1
CUI: C0030567
Disease:
Parkinson Disease 		0.730 GeneticVariation BEFREE The results showed statistically significant association between the dominant model of rs11931532 and PD risk in Asian populations (<i>P</i>=0.006, OR [95% CI]=1.22 [1.06-1.41]). 31118642 2019
dbSNP: rs11931532
rs11931532
Entrez Id: 683
Gene Symbol: BST1
BST1
CUI: C0030567
Disease:
Parkinson Disease 		0.730 GeneticVariation BEFREE Although the rs11931532 variant (T→C) did not show association with PD (OR, 0.99, 95% CI: 0.85-1.15; P=0.9), the pooled estimation of genome-wide association studies (GWAS) showed a significant connection with PD (OR, 1.19, 95% CI: 1.08-1.31; P=0.001). 25986899 2015
dbSNP: rs11931532
rs11931532
Entrez Id: 683
Gene Symbol: BST1
BST1
CUI: C0030567
Disease:
Parkinson Disease 		0.730 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815 2012
dbSNP: rs11931532
rs11931532
Entrez Id: 683
Gene Symbol: BST1
BST1
CUI: C0030567
Disease:
Parkinson Disease 		0.730 GeneticVariation BEFREE SNPs rs11931532 and rs12645693 were not significantly related to sporadic PD. 23026536 2012