rs267607049
|
|
Sucrase-isomaltase deficiency, congenital
|
G |
0.800 |
CausalMutation
|
CLINVAR |
|
|
|
rs121912614
|
|
Sucrase-isomaltase deficiency, congenital
|
T |
0.800 |
CausalMutation
|
CLINVAR |
|
|
|
rs121912613
|
|
Sucrase-isomaltase deficiency, congenital
|
G |
0.800 |
CausalMutation
|
CLINVAR |
|
|
|
rs121912612
|
|
Sucrase-isomaltase deficiency, congenital
|
C |
0.800 |
CausalMutation
|
CLINVAR |
|
|
|
rs121912611
|
|
Sucrase-isomaltase deficiency, congenital
|
G |
0.800 |
CausalMutation
|
CLINVAR |
|
|
|
rs1553775177
|
|
Sucrase-isomaltase deficiency, congenital
|
C |
0.700 |
GeneticVariation
|
CLINVAR |
|
|
|
rs143388292
|
|
Sucrase-isomaltase deficiency, congenital
|
|
0.700 |
GeneticVariation
|
UNIPROT |
|
|
|
rs551975446
|
|
Generalized glycogen storage disease of infants
|
|
0.010 |
GeneticVariation
|
BEFREE |
A de novo 13 nt deletion, a newly identified C647W missense mutation and a deletion of exon 18 in infantile onset glycogen storage disease type II (GSDII).
|
7981676 |
1994 |
rs551975446
|
|
Glycogen storage disease type II
|
|
0.010 |
GeneticVariation
|
BEFREE |
A de novo 13 nt deletion, a newly identified C647W missense mutation and a deletion of exon 18 in infantile onset glycogen storage disease type II (GSDII).
|
7981676 |
1994 |
rs79717168
|
|
Sucrase-isomaltase deficiency, congenital
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Congenital sucrase-isomaltase deficiency. Identification of a glutamine to proline substitution that leads to a transport block of sucrase-isomaltase in a pre-Golgi compartment.
|
8609217 |
1996 |
rs267607049
|
|
Sucrase-isomaltase deficiency, congenital
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Congenital sucrase-isomaltase deficiency. Identification of a glutamine to proline substitution that leads to a transport block of sucrase-isomaltase in a pre-Golgi compartment.
|
8609217 |
1996 |
rs121912616
|
|
Sucrase-isomaltase deficiency, congenital
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Congenital sucrase-isomaltase deficiency. Identification of a glutamine to proline substitution that leads to a transport block of sucrase-isomaltase in a pre-Golgi compartment.
|
8609217 |
1996 |
rs121912615
|
|
Sucrase-isomaltase deficiency, congenital
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Congenital sucrase-isomaltase deficiency. Identification of a glutamine to proline substitution that leads to a transport block of sucrase-isomaltase in a pre-Golgi compartment.
|
8609217 |
1996 |
rs121912614
|
|
Sucrase-isomaltase deficiency, congenital
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Congenital sucrase-isomaltase deficiency. Identification of a glutamine to proline substitution that leads to a transport block of sucrase-isomaltase in a pre-Golgi compartment.
|
8609217 |
1996 |
rs121912613
|
|
Sucrase-isomaltase deficiency, congenital
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Congenital sucrase-isomaltase deficiency. Identification of a glutamine to proline substitution that leads to a transport block of sucrase-isomaltase in a pre-Golgi compartment.
|
8609217 |
1996 |
rs121912612
|
|
Sucrase-isomaltase deficiency, congenital
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Congenital sucrase-isomaltase deficiency. Identification of a glutamine to proline substitution that leads to a transport block of sucrase-isomaltase in a pre-Golgi compartment.
|
8609217 |
1996 |
rs121912611
|
|
Sucrase-isomaltase deficiency, congenital
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Congenital sucrase-isomaltase deficiency. Identification of a glutamine to proline substitution that leads to a transport block of sucrase-isomaltase in a pre-Golgi compartment.
|
8609217 |
1996 |
rs765433197
|
|
Sucrase-isomaltase deficiency, congenital
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Congenital sucrase-isomaltase deficiency. Identification of a glutamine to proline substitution that leads to a transport block of sucrase-isomaltase in a pre-Golgi compartment.
|
8609217 |
1996 |
rs79717168
|
|
Sucrase-isomaltase deficiency, congenital
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Congenital sucrase-isomaltase deficiency arising from cleavage and secretion of a mutant form of the enzyme.
|
10903344 |
2000 |
rs267607049
|
|
Sucrase-isomaltase deficiency, congenital
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Congenital sucrase-isomaltase deficiency arising from cleavage and secretion of a mutant form of the enzyme.
|
10903344 |
2000 |
rs121912616
|
|
Sucrase-isomaltase deficiency, congenital
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Congenital sucrase-isomaltase deficiency arising from cleavage and secretion of a mutant form of the enzyme.
|
10903344 |
2000 |
rs121912615
|
|
Sucrase-isomaltase deficiency, congenital
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Congenital sucrase-isomaltase deficiency arising from cleavage and secretion of a mutant form of the enzyme.
|
10903344 |
2000 |
rs121912614
|
|
Sucrase-isomaltase deficiency, congenital
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Congenital sucrase-isomaltase deficiency arising from cleavage and secretion of a mutant form of the enzyme.
|
10903344 |
2000 |
rs121912613
|
|
Sucrase-isomaltase deficiency, congenital
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Congenital sucrase-isomaltase deficiency arising from cleavage and secretion of a mutant form of the enzyme.
|
10903344 |
2000 |
rs121912612
|
|
Sucrase-isomaltase deficiency, congenital
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Congenital sucrase-isomaltase deficiency arising from cleavage and secretion of a mutant form of the enzyme.
|
10903344 |
2000 |