rs398124626
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
AT
0.700
CausalMutation
CLINVAR
Early-onset limb-girdle muscular dystrophy-2L in a female athlete.
27862037
2017
rs137854529
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
Osteogenesis imperfecta, Levin type
T
0.700
CausalMutation
CLINVAR
Decreased Aerobic Capacity in ANO5-Muscular Dystrophy.
27911336
2016
rs1403946332
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
G
0.700
CausalMutation
CLINVAR
Decreased Aerobic Capacity in ANO5-Muscular Dystrophy.
27911336
2016
rs201725369
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
Osteogenesis imperfecta, Levin type
T
0.700
CausalMutation
CLINVAR
Targeted Re-Sequencing Emulsion PCR Panel for Myopathies: Results in 94 Cases.
27854218
2016
rs281865467
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
Osteogenesis imperfecta, Levin type
0.700
GeneticVariation
UNIPROT
Whole exome sequencing links dental tumor to an autosomal-dominant mutation in ANO5 gene associated with gnathodiaphyseal dysplasia and muscle dystrophies.
27216912
2016
rs878854367
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
A
0.700
GeneticVariation
CLINVAR
Targeted Re-Sequencing Emulsion PCR Panel for Myopathies: Results in 94 Cases.
27854218
2016
rs115750596
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
0.700
GeneticVariation
UNIPROT
Clinical and genetic features of anoctaminopathy in Saudi Arabia.
25864073
2015
rs115750596
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
0.700
GeneticVariation
UNIPROT
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations.
25891276
2015
rs137854523
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
Hereditary fructose intolerance syndrome
T
0.700
CausalMutation
CLINVAR
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations.
25891276
2015
rs137854523
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
Osteogenesis imperfecta, Levin type
T
0.700
GeneticVariation
CLINVAR
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations.
25891276
2015
rs138144479
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
0.700
GeneticVariation
UNIPROT
Clinical and genetic features of anoctaminopathy in Saudi Arabia.
25864073
2015
rs138144479
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
0.700
GeneticVariation
UNIPROT
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations.
25891276
2015
rs139618850
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
0.700
GeneticVariation
UNIPROT
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations.
25891276
2015
rs139618850
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
0.700
GeneticVariation
UNIPROT
Clinical and genetic features of anoctaminopathy in Saudi Arabia.
25864073
2015
rs142027093
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
Osteogenesis imperfecta, Levin type
A
0.700
CausalMutation
CLINVAR
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations.
25891276
2015
rs142027093
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
A
0.700
CausalMutation
CLINVAR
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations.
25891276
2015
rs142073798
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
0.700
GeneticVariation
UNIPROT
Clinical and genetic features of anoctaminopathy in Saudi Arabia.
25864073
2015
rs142073798
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
0.700
GeneticVariation
UNIPROT
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations.
25891276
2015
rs1422717390
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
0.700
GeneticVariation
UNIPROT
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations.
25891276
2015
rs1422717390
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
0.700
GeneticVariation
UNIPROT
Clinical and genetic features of anoctaminopathy in Saudi Arabia.
25864073
2015
rs148293985
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
0.700
GeneticVariation
UNIPROT
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations.
25891276
2015
rs148293985
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
0.700
GeneticVariation
UNIPROT
Clinical and genetic features of anoctaminopathy in Saudi Arabia.
25864073
2015
rs1554930314
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
T
0.700
GeneticVariation
CLINVAR
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations.
25891276
2015
rs200631556
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
0.700
GeneticVariation
UNIPROT
Clinical and genetic features of anoctaminopathy in Saudi Arabia.
25864073
2015
rs200631556
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
0.700
GeneticVariation
UNIPROT
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations.
25891276
2015