Gene: DES ×
Source: UNIPROT ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs59308628
rs59308628
DES
0.700 GeneticVariation UNIPROT

dbSNP: rs60794845
rs60794845
DES
0.700 GeneticVariation UNIPROT

dbSNP: rs903985237
rs903985237
DES
0.700 GeneticVariation UNIPROT

dbSNP: rs121913004
rs121913004
DES
0.810 GeneticVariation UNIPROT Missense mutations in desmin associated with familial cardiac and skeletal myopathy. 9697706

1998
dbSNP: rs267607482
rs267607482
DES
0.810 GeneticVariation UNIPROT Missense mutations in desmin associated with familial cardiac and skeletal myopathy. 9697706

1998
dbSNP: rs267607490
rs267607490
DES
0.810 GeneticVariation UNIPROT Missense mutations in desmin associated with familial cardiac and skeletal myopathy. 9697706

1998
dbSNP: rs121913000
rs121913000
DES
0.800 GeneticVariation UNIPROT Missense mutations in desmin associated with familial cardiac and skeletal myopathy. 9697706

1998
dbSNP: rs121913001
rs121913001
DES
0.800 GeneticVariation UNIPROT Missense mutations in desmin associated with familial cardiac and skeletal myopathy. 9697706

1998
dbSNP: rs121913003
rs121913003
DES
0.800 GeneticVariation UNIPROT Missense mutations in desmin associated with familial cardiac and skeletal myopathy. 9697706

1998
dbSNP: rs121913005
rs121913005
DES
0.800 GeneticVariation UNIPROT Missense mutations in desmin associated with familial cardiac and skeletal myopathy. 9697706

1998
dbSNP: rs267607499
rs267607499
DES
0.800 GeneticVariation UNIPROT Missense mutations in desmin associated with familial cardiac and skeletal myopathy. 9697706

1998
dbSNP: rs57496341
rs57496341
DES
0.800 GeneticVariation UNIPROT Missense mutations in desmin associated with familial cardiac and skeletal myopathy. 9697706

1998
dbSNP: rs57639980
rs57639980
DES
0.800 GeneticVariation UNIPROT Missense mutations in desmin associated with familial cardiac and skeletal myopathy. 9697706

1998
dbSNP: rs57955682
rs57955682
DES
0.800 GeneticVariation UNIPROT Missense mutations in desmin associated with familial cardiac and skeletal myopathy. 9697706

1998
dbSNP: rs62635763
rs62635763
DES
0.800 GeneticVariation UNIPROT Missense mutations in desmin associated with familial cardiac and skeletal myopathy. 9697706

1998
dbSNP: rs62636495
rs62636495
DES
0.800 GeneticVariation UNIPROT Missense mutations in desmin associated with familial cardiac and skeletal myopathy. 9697706

1998
dbSNP: rs267607485
rs267607485
DES
0.710 GeneticVariation UNIPROT Missense mutations in desmin associated with familial cardiac and skeletal myopathy. 9697706

1998
dbSNP: rs267607486
rs267607486
DES
0.710 GeneticVariation UNIPROT Missense mutations in desmin associated with familial cardiac and skeletal myopathy. 9697706

1998
dbSNP: rs121913002
rs121913002
DES
0.700 GeneticVariation UNIPROT Missense mutations in desmin associated with familial cardiac and skeletal myopathy. 9697706

1998
dbSNP: rs267607488
rs267607488
DES
0.700 GeneticVariation UNIPROT Missense mutations in desmin associated with familial cardiac and skeletal myopathy. 9697706

1998
dbSNP: rs267607491
rs267607491
DES
0.700 GeneticVariation UNIPROT Missense mutations in desmin associated with familial cardiac and skeletal myopathy. 9697706

1998
dbSNP: rs57694264
rs57694264
DES
0.700 GeneticVariation UNIPROT Missense mutations in desmin associated with familial cardiac and skeletal myopathy. 9697706

1998
dbSNP: rs58898021
rs58898021
DES
0.700 GeneticVariation UNIPROT Missense mutations in desmin associated with familial cardiac and skeletal myopathy. 9697706

1998
dbSNP: rs58999456
rs58999456
DES
0.700 GeneticVariation UNIPROT Missense mutations in desmin associated with familial cardiac and skeletal myopathy. 9697706

1998
dbSNP: rs60798368
rs60798368
DES
0.700 GeneticVariation UNIPROT Missense mutations in desmin associated with familial cardiac and skeletal myopathy. 9697706

1998