Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs731236
rs731236
VDR
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.030 GeneticVariation BEFREE Epidemiological evidence on the relationships between the vitamin D receptor (VDR) single nucleotide polymorphisms (SNPs) rs731236 (TaqI), rs7975232 (ApaI), rs1544410 (BsmI), and rs2228570 (FokI) and Parkinson's disease (PD) is inconsistent. 28216333

2017
dbSNP: rs731236
rs731236
VDR
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.030 GeneticVariation BEFREE Homozygotes for the rs731236 TT (major allele) genotype had a 31% lower risk of PD risk (OR=0.69; 95% CI=0.49, 0.98; p=0.04 for TT vs. TC+CC). 25890641

2015
dbSNP: rs731236
rs731236
VDR
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.030 GeneticVariation BEFREE There were no significant differences in the genotype and allele frequencies of VDR rs4334089 and rs731236 polymorphisms between the group of patients with PD and the control group in a Chinese Han population (for VDR rs4334089: OR 1.02, 95% CI: 0.85-1.23; for VDR rs731236: OR 1.13, 95% CI: 0.75-1.71). 22947263

2013