Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894844
rs104894844
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
A 0.700 CausalMutation CLINVAR Nature and frequency of mutations in the alpha-galactosidase A gene that cause Fabry disease. 7504405

1993

dbSNP: rs104894847
rs104894847
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 GeneticVariation UNIPROT Alpha-Galactosidase A p.A143T, a non-Fabry disease-causing variant. 27142856

2016

dbSNP: rs104894847
rs104894847
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 GeneticVariation UNIPROT Functional and Clinical Consequences of Novel α-Galactosidase A Mutations in Fabry Disease. 26415523

2016

dbSNP: rs104894847
rs104894847
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 GeneticVariation UNIPROT Analysis of splice-site mutations of the alpha-galactosidase A gene in Fabry disease. 12786754

2003

dbSNP: rs104894847
rs104894847
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 GeneticVariation UNIPROT Identification of a novel de novo mutation (G373D) in the alpha-galactosidase A gene (GLA) in a patient affected with Fabry disease. 11295840

2001

dbSNP: rs104894847
rs104894847
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 GeneticVariation UNIPROT Characterization of two alpha-galactosidase mutants (Q279E and R301Q) found in an atypical variant of Fabry disease. 10838196

2000

dbSNP: rs104894847
rs104894847
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 GeneticVariation UNIPROT Identification of four novel mutations in five unrelated Korean families with Fabry disease. 11076046

2000

dbSNP: rs104894847
rs104894847
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 GeneticVariation UNIPROT Twenty novel mutations in the alpha-galactosidase A gene causing Fabry disease. 10666480

1999

dbSNP: rs104894847
rs104894847
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 GeneticVariation UNIPROT Fabry disease: identification of novel alpha-galactosidase A mutations and molecular carrier detection by use of fluorescent chemical cleavage of mismatches. 10208848

1999

dbSNP: rs104894847
rs104894847
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 GeneticVariation UNIPROT Novel missense mutation (M72V) of alpha-galactosidase gene and its expression product in an atypical Fabry hemizygote. 9452090

1998

dbSNP: rs104894847
rs104894847
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 GeneticVariation UNIPROT Mutation analysis in 11 French patients with Fabry disease. 9452111

1998

dbSNP: rs104894847
rs104894847
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 GeneticVariation UNIPROT Screening and detection of gene mutations in Japanese patients with Fabry disease by non-radioactive single-stranded conformation polymorphism analysis. 9105656

1997

dbSNP: rs104894847
rs104894847
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 GeneticVariation UNIPROT An atypical variant of Fabry's disease in men with left ventricular hypertrophy. 7596372

1995

dbSNP: rs104894847
rs104894847
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 GeneticVariation UNIPROT Alpha-galactosidase gene mutations in Fabry disease: heterogeneous expressions of mutant enzyme proteins. 7759078

1995

dbSNP: rs104894847
rs104894847
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 GeneticVariation UNIPROT Detection of 8 new mutations in the alpha-galactosidase A gene in Fabry disease. 8069316

1994

dbSNP: rs104894847
rs104894847
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 GeneticVariation UNIPROT Nature and frequency of mutations in the alpha-galactosidase A gene that cause Fabry disease. 7504405

1993

dbSNP: rs104894847
rs104894847
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 GeneticVariation UNIPROT Point mutations in the upstream region of the alpha-galactosidase A gene exon 6 in an atypical variant of Fabry disease. 1315715

1992

dbSNP: rs104894847
rs104894847
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 GeneticVariation UNIPROT An atypical variant of Fabry's disease with manifestations confined to the myocardium. 1846223

1991

dbSNP: rs104894847
rs104894847
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 GeneticVariation UNIPROT A case of Fabry's disease in a patient with no alpha-galactosidase A activity caused by a single amino acid substitution of Pro-40 by Ser. 2152885

1990

dbSNP: rs104894847
rs104894847
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 GeneticVariation UNIPROT Identification of point mutations in the alpha-galactosidase A gene in classical and atypical hemizygotes with Fabry disease. 2171331

1990

dbSNP: rs104894847
rs104894847
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 GeneticVariation UNIPROT Fabry disease: six gene rearrangements and an exonic point mutation in the alpha-galactosidase gene. 2539398

1989

dbSNP: rs104894849
rs104894849
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057516429
rs1057516429
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057519609
rs1057519609
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057521047
rs1057521047
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 GeneticVariation UNIPROT