Gene: GBE1 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137852886
rs137852886
GBE1
G 0.800 CausalMutation CLINVAR

dbSNP: rs137852887
rs137852887
GBE1
T 0.800 CausalMutation CLINVAR

dbSNP: rs137852889
rs137852889
GBE1
C 0.800 CausalMutation CLINVAR

dbSNP: rs137852888
rs137852888
GBE1
A 0.710 CausalMutation CLINVAR

dbSNP: rs80338671
rs80338671
GBE1
C 0.710 CausalMutation CLINVAR

dbSNP: rs137852890
rs137852890
GBE1
A 0.700 CausalMutation CLINVAR

dbSNP: rs137852894
rs137852894
GBE1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1553690406
rs1553690406
GBE1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1559637815
rs1559637815
GBE1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs397515343
rs397515343
GBE1
T 0.700 CausalMutation CLINVAR

dbSNP: rs397515344
rs397515344
GBE1
G 0.700 CausalMutation CLINVAR

dbSNP: rs763016962
rs763016962
GBE1
A 0.700 CausalMutation CLINVAR

dbSNP: rs80338672
rs80338672
GBE1
A 0.700 CausalMutation CLINVAR

dbSNP: rs80338673
rs80338673
GBE1
T 0.700 CausalMutation CLINVAR

dbSNP: rs137852886
rs137852886
GBE1
G 0.800 GeneticVariation CLINVAR Hepatic and neuromuscular forms of glycogen storage disease type IV caused by mutations in the same glycogen-branching enzyme gene. 8613547

1996
dbSNP: rs137852886
rs137852886
GBE1
0.800 GeneticVariation UNIPROT Hepatic and neuromuscular forms of glycogen storage disease type IV caused by mutations in the same glycogen-branching enzyme gene. 8613547

1996
dbSNP: rs137852887
rs137852887
GBE1
0.800 GeneticVariation UNIPROT Hepatic and neuromuscular forms of glycogen storage disease type IV caused by mutations in the same glycogen-branching enzyme gene. 8613547

1996
dbSNP: rs137852889
rs137852889
GBE1
0.800 GeneticVariation UNIPROT Hepatic and neuromuscular forms of glycogen storage disease type IV caused by mutations in the same glycogen-branching enzyme gene. 8613547

1996
dbSNP: rs80338671
rs80338671
GBE1
C 0.710 GeneticVariation CLINVAR The Y329S allele was also detected in another patient with the nonprogressive form of GSD-IV but not in 35 unrelated controls or in patients with the more severe forms of GSD-IV. 8613547

1996
dbSNP: rs80338671
rs80338671
GBE1
0.710 GeneticVariation BEFREE The Y329S allele was also detected in another patient with the nonprogressive form of GSD-IV but not in 35 unrelated controls or in patients with the more severe forms of GSD-IV. 8613547

1996
dbSNP: rs80338671
rs80338671
GBE1
G 0.710 CausalMutation CLINVAR The Y329S allele was also detected in another patient with the nonprogressive form of GSD-IV but not in 35 unrelated controls or in patients with the more severe forms of GSD-IV. 8613547

1996
dbSNP: rs137852891
rs137852891
GBE1
0.700 GeneticVariation UNIPROT Hepatic and neuromuscular forms of glycogen storage disease type IV caused by mutations in the same glycogen-branching enzyme gene. 8613547

1996
dbSNP: rs80338671
rs80338671
GBE1
G 0.710 CausalMutation CLINVAR Adult polyglucosan body disease in Ashkenazi Jewish patients carrying the Tyr329Ser mutation in the glycogen-branching enzyme gene. 9851430

1998
dbSNP: rs192044702
rs192044702
GBE1
G 0.700 CausalMutation CLINVAR Adult polyglucosan body disease in Ashkenazi Jewish patients carrying the Tyr329Ser mutation in the glycogen-branching enzyme gene. 9851430

1998
dbSNP: rs137852886
rs137852886
GBE1
0.800 GeneticVariation UNIPROT A novel missense mutation in the glycogen branching enzyme gene in a child with myopathy and hepatopathy. 10545044

1999