Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893877
rs104893877
SNCA
0.800 GeneticVariation UNIPROT Molecular determinants of α-synuclein mutants' oligomerization and membrane interactions. 25561023

2015
dbSNP: rs104893878
rs104893878
SNCA ; SNCA-AS1
0.800 GeneticVariation UNIPROT Molecular determinants of α-synuclein mutants' oligomerization and membrane interactions. 25561023

2015
dbSNP: rs104893877
rs104893877
SNCA
0.800 GeneticVariation UNIPROT The H50Q mutation enhances α-synuclein aggregation, secretion, and toxicity. 24936070

2014
dbSNP: rs104893878
rs104893878
SNCA ; SNCA-AS1
0.800 GeneticVariation UNIPROT The H50Q mutation enhances α-synuclein aggregation, secretion, and toxicity. 24936070

2014
dbSNP: rs104893877
rs104893877
SNCA
0.800 GeneticVariation UNIPROT A novel α-synuclein missense mutation in Parkinson disease. 23427326

2013
dbSNP: rs104893877
rs104893877
SNCA
0.800 GeneticVariation UNIPROT Alpha-synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease. 23457019

2013
dbSNP: rs104893878
rs104893878
SNCA ; SNCA-AS1
0.800 GeneticVariation UNIPROT A novel α-synuclein missense mutation in Parkinson disease. 23427326

2013
dbSNP: rs104893878
rs104893878
SNCA ; SNCA-AS1
0.800 GeneticVariation UNIPROT Alpha-synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease. 23457019

2013
dbSNP: rs104893877
rs104893877
SNCA
0.800 GeneticVariation UNIPROT The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementia. 14755719

2004
dbSNP: rs104893878
rs104893878
SNCA ; SNCA-AS1
0.800 GeneticVariation UNIPROT The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementia. 14755719

2004
dbSNP: rs104893877
rs104893877
SNCA
0.800 GeneticVariation UNIPROT Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease. 9462735

1998
dbSNP: rs104893878
rs104893878
SNCA ; SNCA-AS1
0.800 GeneticVariation UNIPROT Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease. 9462735

1998
dbSNP: rs104893877
rs104893877
SNCA
0.800 GeneticVariation UNIPROT Mutation in the alpha-synuclein gene identified in families with Parkinson's disease. 9197268

1997
dbSNP: rs104893878
rs104893878
SNCA ; SNCA-AS1
0.800 GeneticVariation UNIPROT Mutation in the alpha-synuclein gene identified in families with Parkinson's disease. 9197268

1997
dbSNP: rs104893877
rs104893877
SNCA
T 0.800 CausalMutation CLINVAR

dbSNP: rs104893878
rs104893878
SNCA ; SNCA-AS1
G 0.800 CausalMutation CLINVAR

dbSNP: rs104893875
rs104893875
SNCA
0.700 GeneticVariation UNIPROT Molecular determinants of α-synuclein mutants' oligomerization and membrane interactions. 25561023

2015
dbSNP: rs201106962
rs201106962
SNCA
0.700 GeneticVariation UNIPROT Molecular determinants of α-synuclein mutants' oligomerization and membrane interactions. 25561023

2015
dbSNP: rs104893875
rs104893875
SNCA
0.700 GeneticVariation UNIPROT The H50Q mutation enhances α-synuclein aggregation, secretion, and toxicity. 24936070

2014
dbSNP: rs201106962
rs201106962
SNCA
0.700 GeneticVariation UNIPROT The H50Q mutation enhances α-synuclein aggregation, secretion, and toxicity. 24936070

2014
dbSNP: rs104893875
rs104893875
SNCA
0.700 GeneticVariation UNIPROT A novel α-synuclein missense mutation in Parkinson disease. 23427326

2013
dbSNP: rs104893875
rs104893875
SNCA
0.700 GeneticVariation UNIPROT Alpha-synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease. 23457019

2013
dbSNP: rs201106962
rs201106962
SNCA
0.700 GeneticVariation UNIPROT Alpha-synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease. 23457019

2013
dbSNP: rs201106962
rs201106962
SNCA
0.700 GeneticVariation UNIPROT A novel α-synuclein missense mutation in Parkinson disease. 23427326

2013
dbSNP: rs104893875
rs104893875
SNCA
0.700 GeneticVariation UNIPROT The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementia. 14755719

2004