Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 859
Gene Symbol: CAV3
CAV3 		0.700 CausalMutation phenotype CLINVAR
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 5310
Gene Symbol: PKD1
PKD1 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 285489
Gene Symbol: DOK7
DOK7 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 54332
Gene Symbol: GDAP1
GDAP1 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 203859
Gene Symbol: ANO5
ANO5 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 29925
Gene Symbol: GMPPB
GMPPB 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 79147
Gene Symbol: FKRP
FKRP 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 51066
Gene Symbol: SSUH2
SSUH2 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 23245
Gene Symbol: ASTN2
ASTN2 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 6442
Gene Symbol: SGCA
SGCA 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 8291
Gene Symbol: DYSF
DYSF 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 29888
Gene Symbol: STRN4
STRN4 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 26092
Gene Symbol: TOR1AIP1
TOR1AIP1 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 6786
Gene Symbol: STIM1
STIM1 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 203859
Gene Symbol: ANO5
ANO5 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 6329
Gene Symbol: SCN4A
SCN4A 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 128989
Gene Symbol: TANGO2
TANGO2 		0.100 CausalMutation phenotype CLINVAR Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 Mutations. 26805781 2016
Entrez Id: 1756
Gene Symbol: DMD
DMD 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 8557
Gene Symbol: TCAP
TCAP 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 1756
Gene Symbol: DMD
DMD 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 8291
Gene Symbol: DYSF
DYSF 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 22954
Gene Symbol: TRIM32
TRIM32 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 825
Gene Symbol: CAPN3
CAPN3 		0.100 CausalMutation phenotype CLINVAR