rs121909297
×
Entrez Id:
6444
Gene Symbol:
SGCD
SGCD
Limb-girdle muscular dystrophy type 2F
A
0.800
CausalMutation
CLINVAR
rs121909296
×
Entrez Id:
6444
Gene Symbol:
SGCD
SGCD
Limb-girdle muscular dystrophy type 2F
A
0.700
CausalMutation
CLINVAR
rs1267810339
×
Entrez Id:
6444
Gene Symbol:
SGCD
SGCD
Limb-girdle muscular dystrophy type 2F
A
0.700
GeneticVariation
CLINVAR
rs1267810339
×
Entrez Id:
6444
Gene Symbol:
SGCD
SGCD
CARDIOMYOPATHY, DILATED, 1L
A
0.700
GeneticVariation
CLINVAR
rs1554094947
×
Entrez Id:
6444
Gene Symbol:
SGCD
SGCD
Limb-girdle muscular dystrophy type 2F
AGGTG
0.700
CausalMutation
CLINVAR
rs1554137109
×
Entrez Id:
6444
Gene Symbol:
SGCD
SGCD
CARDIOMYOPATHY, DILATED, 1L
C
0.700
GeneticVariation
CLINVAR
rs1554137109
×
Entrez Id:
6444
Gene Symbol:
SGCD
SGCD
Limb-girdle muscular dystrophy type 2F
C
0.700
GeneticVariation
CLINVAR
rs1554137130
×
Entrez Id:
6444
Gene Symbol:
SGCD
SGCD
CARDIOMYOPATHY, DILATED, 1L
T
0.700
GeneticVariation
CLINVAR
rs1554137130
×
Entrez Id:
6444
Gene Symbol:
SGCD
SGCD
Limb-girdle muscular dystrophy type 2F
T
0.700
GeneticVariation
CLINVAR
rs267607045
×
Entrez Id:
6444
Gene Symbol:
SGCD
SGCD
Limb-girdle muscular dystrophy type 2F
C
0.700
CausalMutation
CLINVAR
rs397517921
×
Entrez Id:
6444
Gene Symbol:
SGCD
SGCD
Neuromuscular Diseases
C
0.700
GeneticVariation
CLINVAR
rs397517923
×
Entrez Id:
6444
Gene Symbol:
SGCD
SGCD
Limb-girdle muscular dystrophy type 2F
A
0.700
GeneticVariation
CLINVAR
rs397517923
×
Entrez Id:
6444
Gene Symbol:
SGCD
SGCD
CARDIOMYOPATHY, DILATED, 1L
A
0.700
GeneticVariation
CLINVAR
rs727503422
×
Entrez Id:
6444
Gene Symbol:
SGCD
SGCD
CARDIOMYOPATHY, DILATED, 1L
A
0.700
GeneticVariation
CLINVAR
rs727503422
×
Entrez Id:
6444
Gene Symbol:
SGCD
SGCD
Limb-girdle muscular dystrophy type 2F
A
0.700
GeneticVariation
CLINVAR
rs727503422
×
Entrez Id:
6444
Gene Symbol:
SGCD
SGCD
Neuromuscular Diseases
A
0.700
GeneticVariation
CLINVAR
rs1554094927
×
Entrez Id:
6444
Gene Symbol:
SGCD
SGCD
Limb-girdle muscular dystrophy type 2F
A
0.700
CausalMutation
CLINVAR
Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene.
8841194
1996
rs121909295
×
Entrez Id:
6444
Gene Symbol:
SGCD
SGCD
Limb-girdle muscular dystrophy type 2F
T
0.700
CausalMutation
CLINVAR
Mutations in the delta-sarcoglycan gene are a rare cause of autosomal recessive limb-girdle muscular dystrophy (LGMD2).
10735275
1997
rs121909295
×
Entrez Id:
6444
Gene Symbol:
SGCD
SGCD
CARDIOMYOPATHY, DILATED, 1L
T
0.700
CausalMutation
CLINVAR
Mutations in the delta-sarcoglycan gene are a rare cause of autosomal recessive limb-girdle muscular dystrophy (LGMD2).
10735275
1997
rs1554094927
×
Entrez Id:
6444
Gene Symbol:
SGCD
SGCD
Limb-girdle muscular dystrophy type 2F
A
0.700
CausalMutation
CLINVAR
Mutations in the delta-sarcoglycan gene are a rare cause of autosomal recessive limb-girdle muscular dystrophy (LGMD2).
10735275
1997
rs121909297
×
Entrez Id:
6444
Gene Symbol:
SGCD
SGCD
Limb-girdle muscular dystrophy type 2F
0.800
GeneticVariation
UNIPROT
A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies.
9832045
1998
rs121909298
×
Entrez Id:
6444
Gene Symbol:
SGCD
SGCD
CARDIOMYOPATHY, DILATED, 1L
0.700
GeneticVariation
UNIPROT
Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy.
10974018
2000
rs1554094927
×
Entrez Id:
6444
Gene Symbol:
SGCD
SGCD
Limb-girdle muscular dystrophy type 2F
A
0.700
CausalMutation
CLINVAR
A homozygous nonsense mutation in delta-sarcoglycan exon 3 in a case of LGMD2F.
10838250
2000
rs1175344271
×
Entrez Id:
6444
Gene Symbol:
SGCD
SGCD
CARDIOMYOPATHY, DILATED, 1L
A
0.700
GeneticVariation
CLINVAR
Identification of functional domains in sarcoglycans essential for their interaction and plasma membrane targeting.
16524571
2006
rs1175344271
×
Entrez Id:
6444
Gene Symbol:
SGCD
SGCD
Limb-girdle muscular dystrophy type 2F
A
0.700
GeneticVariation
CLINVAR
Identification of functional domains in sarcoglycans essential for their interaction and plasma membrane targeting.
16524571
2006