rs104894293
|
Entrez Id: |
5913 |
Gene Symbol: |
RAPSN |
RAPSN
|
MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
|
G |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs104894294
|
Entrez Id: |
5913 |
Gene Symbol: |
RAPSN |
RAPSN
|
MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
|
A |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs104894299
|
Entrez Id: |
5913 |
Gene Symbol: |
RAPSN |
RAPSN
|
MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
|
T |
0.800 |
GeneticVariation |
CLINVAR |
|
|
|
rs104894300
|
Entrez Id: |
5913 |
Gene Symbol: |
RAPSN |
RAPSN
|
MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
|
G |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs121909254
|
Entrez Id: |
5913 |
Gene Symbol: |
RAPSN |
RAPSN
|
MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
|
T |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs121909255
|
Entrez Id: |
5913 |
Gene Symbol: |
RAPSN |
RAPSN
|
MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
|
T |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs104894294
|
Entrez Id: |
5913 |
Gene Symbol: |
RAPSN |
RAPSN
|
Myopathy
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs104894299
|
Entrez Id: |
5913 |
Gene Symbol: |
RAPSN |
RAPSN
|
Myopathy
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs104894299
|
Entrez Id: |
5913 |
Gene Symbol: |
RAPSN |
RAPSN
|
Pena-Shokeir syndrome type I
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs104894301
|
Entrez Id: |
5913 |
Gene Symbol: |
RAPSN |
RAPSN
|
MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1479498379
|
Entrez Id: |
5913 |
Gene Symbol: |
RAPSN |
RAPSN
|
MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1479498379
|
Entrez Id: |
5913 |
Gene Symbol: |
RAPSN |
RAPSN
|
Pena-Shokeir syndrome type I
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1555142603
|
Entrez Id: |
5913 |
Gene Symbol: |
RAPSN |
RAPSN
|
Pena-Shokeir syndrome type I
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1555142603
|
Entrez Id: |
5913 |
Gene Symbol: |
RAPSN |
RAPSN
|
MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs45547231
|
Entrez Id: |
5913 |
Gene Symbol: |
RAPSN |
RAPSN
|
MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs786200904
|
Entrez Id: |
5913 |
Gene Symbol: |
RAPSN |
RAPSN
|
MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
|
AAGAAC |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs786205885
|
Entrez Id: |
5913 |
Gene Symbol: |
RAPSN |
RAPSN
|
MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
|
TAG |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs104894293
|
Entrez Id: |
5913 |
Gene Symbol: |
RAPSN |
RAPSN
|
MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
|
|
0.800 |
GeneticVariation |
UNIPROT |
Rapsyn mutations in humans cause endplate acetylcholine-receptor deficiency and myasthenic syndrome.
|
11791205 |
2002 |
rs104894294
|
Entrez Id: |
5913 |
Gene Symbol: |
RAPSN |
RAPSN
|
MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
|
|
0.800 |
GeneticVariation |
UNIPROT |
Rapsyn mutations in humans cause endplate acetylcholine-receptor deficiency and myasthenic syndrome.
|
11791205 |
2002 |
rs104894299
|
Entrez Id: |
5913 |
Gene Symbol: |
RAPSN |
RAPSN
|
MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
|
|
0.800 |
GeneticVariation |
UNIPROT |
Rapsyn mutations in humans cause endplate acetylcholine-receptor deficiency and myasthenic syndrome.
|
11791205 |
2002 |
rs104894299
|
Entrez Id: |
5913 |
Gene Symbol: |
RAPSN |
RAPSN
|
MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
|
T |
0.800 |
CausalMutation |
CLINVAR |
Rapsyn mutations in humans cause endplate acetylcholine-receptor deficiency and myasthenic syndrome.
|
11791205 |
2002 |
rs104894300
|
Entrez Id: |
5913 |
Gene Symbol: |
RAPSN |
RAPSN
|
MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
|
|
0.800 |
GeneticVariation |
UNIPROT |
Rapsyn mutations in humans cause endplate acetylcholine-receptor deficiency and myasthenic syndrome.
|
11791205 |
2002 |
rs121909254
|
Entrez Id: |
5913 |
Gene Symbol: |
RAPSN |
RAPSN
|
MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
|
|
0.800 |
GeneticVariation |
UNIPROT |
Rapsyn mutations in humans cause endplate acetylcholine-receptor deficiency and myasthenic syndrome.
|
11791205 |
2002 |
rs121909255
|
Entrez Id: |
5913 |
Gene Symbol: |
RAPSN |
RAPSN
|
MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
|
|
0.800 |
GeneticVariation |
UNIPROT |
Rapsyn mutations in humans cause endplate acetylcholine-receptor deficiency and myasthenic syndrome.
|
11791205 |
2002 |
rs104894299
|
Entrez Id: |
5913 |
Gene Symbol: |
RAPSN |
RAPSN
|
Pena-Shokeir syndrome type I
|
T |
0.700 |
CausalMutation |
CLINVAR |
Rapsyn mutations in humans cause endplate acetylcholine-receptor deficiency and myasthenic syndrome.
|
11791205 |
2002 |