Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1438259227
rs1438259227
PRKN
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.020 GeneticVariation BEFREE The A53T mutation in the SNCA gene, although uncommon, does represent a cause of PD in the Greek population, especially of familial EOPD with autosomal dominant inheritance. 24313877

2014
dbSNP: rs1438259227
rs1438259227
PRKN
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.020 GeneticVariation BEFREE A missense mutation of SNCA (A53T) was found in a familial PD with autosomal dominant inheritance. 18704525

2008