Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199922550
rs199922550
Entrez Id: 29925;63891
Gene Symbol: GMPPB;RNF123
GMPPB;RNF123
CUI: C3714932
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14
0.800 GeneticVariation UNIPROT
dbSNP: rs199922550
rs199922550
Entrez Id: 29925;63891
Gene Symbol: GMPPB;RNF123
GMPPB;RNF123
CUI: C3714932
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14
T 0.800 CausalMutation CLINVAR
dbSNP: rs202160208
rs202160208
Entrez Id: 29925
Gene Symbol: GMPPB
GMPPB
CUI: C3714932
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14
0.800 GeneticVariation UNIPROT
dbSNP: rs397509424
rs397509424
Entrez Id: 29925
Gene Symbol: GMPPB
GMPPB
CUI: C3714932
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14
A 0.800 CausalMutation CLINVAR
dbSNP: rs771861177
rs771861177
Entrez Id: 29925;63891
Gene Symbol: GMPPB;RNF123
GMPPB;RNF123
CUI: C3714932
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14
0.800 GeneticVariation UNIPROT
dbSNP: rs875989850
rs875989850
Entrez Id: 29925
Gene Symbol: GMPPB
GMPPB
CUI: C3714932
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14
T 0.800 CausalMutation CLINVAR
dbSNP: rs1064796834
rs1064796834
Entrez Id: 29925;63891
Gene Symbol: GMPPB;RNF123
GMPPB;RNF123
CUI: C3714932
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14
0.700 GeneticVariation UNIPROT
dbSNP: rs145535498
rs145535498
Entrez Id: 29925
Gene Symbol: GMPPB
GMPPB
CUI: C3714932
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14
0.700 GeneticVariation UNIPROT
dbSNP: rs1553691918
rs1553691918
Entrez Id: 29925
Gene Symbol: GMPPB
GMPPB
CUI: C3714932
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14
C 0.700 CausalMutation CLINVAR
dbSNP: rs1553691975
rs1553691975
Entrez Id: 29925
Gene Symbol: GMPPB
GMPPB
CUI: C3714932
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14
ACT 0.700 CausalMutation CLINVAR
dbSNP: rs397509422
rs397509422
Entrez Id: 29925;63891
Gene Symbol: GMPPB;RNF123
GMPPB;RNF123
CUI: C3714932
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14
T 0.700 CausalMutation CLINVAR
dbSNP: rs397509425
rs397509425
Entrez Id: 29925
Gene Symbol: GMPPB
GMPPB
CUI: C3714932
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14
A 0.700 CausalMutation CLINVAR
dbSNP: rs397509426
rs397509426
Entrez Id: 29925
Gene Symbol: GMPPB
GMPPB
CUI: C3714932
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14
A 0.700 CausalMutation CLINVAR
dbSNP: rs756682220
rs756682220
Entrez Id: 29925
Gene Symbol: GMPPB
GMPPB
CUI: C3714932
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14
0.700 GeneticVariation UNIPROT
dbSNP: rs763971677
rs763971677
Entrez Id: 29925
Gene Symbol: GMPPB
GMPPB
CUI: C3714932
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14
A 0.700 CausalMutation CLINVAR
dbSNP: rs875989851
rs875989851
Entrez Id: 29925
Gene Symbol: GMPPB
GMPPB
CUI: C3714932
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14
A 0.700 CausalMutation CLINVAR
dbSNP: rs142336618
rs142336618
Entrez Id: 29925
Gene Symbol: GMPPB
GMPPB
CUI: C3714932
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14
0.800 GeneticVariation UNIPROT Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycan. 23768512 2013
dbSNP: rs142336618
rs142336618
Entrez Id: 29925
Gene Symbol: GMPPB
GMPPB
CUI: C3714932
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14
G 0.800 CausalMutation CLINVAR Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycan. 23768512 2013
dbSNP: rs142908436
rs142908436
Entrez Id: 29925
Gene Symbol: GMPPB
GMPPB
CUI: C3714932
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14
0.800 GeneticVariation UNIPROT Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycan. 23768512 2013
dbSNP: rs199922550
rs199922550
Entrez Id: 29925;63891
Gene Symbol: GMPPB;RNF123
GMPPB;RNF123
CUI: C3714932
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14
T 0.800 GeneticVariation CLINVAR Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycan. 23768512 2013
dbSNP: rs202160208
rs202160208
Entrez Id: 29925
Gene Symbol: GMPPB
GMPPB
CUI: C3714932
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14
T 0.800 CausalMutation CLINVAR Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycan. 23768512 2013
dbSNP: rs397509424
rs397509424
Entrez Id: 29925
Gene Symbol: GMPPB
GMPPB
CUI: C3714932
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14
0.800 GeneticVariation UNIPROT Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycan. 23768512 2013
dbSNP: rs761714818
rs761714818
Entrez Id: 29925
Gene Symbol: GMPPB
GMPPB
CUI: C3714932
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14
0.800 GeneticVariation UNIPROT Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycan. 23768512 2013
dbSNP: rs875989850
rs875989850
Entrez Id: 29925
Gene Symbol: GMPPB
GMPPB
CUI: C3714932
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14
0.800 GeneticVariation UNIPROT Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycan. 23768512 2013
dbSNP: rs145564018
rs145564018
Entrez Id: 29925
Gene Symbol: GMPPB
GMPPB
CUI: C3714932
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14
T 0.700 GeneticVariation CLINVAR Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycan. 23768512 2013