Gene: DSP ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121912997
rs121912997
DSP
T 0.700 GeneticVariation CLINVAR

dbSNP: rs148894066
rs148894066
DSP
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1554105614
rs1554105614
DSP
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1554108012
rs1554108012
DSP
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1554108152
rs1554108152
DSP
GGAAAATC 0.700 GeneticVariation CLINVAR

dbSNP: rs1554108287
rs1554108287
DSP
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1554108431
rs1554108431
DSP
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1561703922
rs1561703922
DSP
A 0.700 GeneticVariation CLINVAR

dbSNP: rs397516927
rs397516927
DSP
CA 0.700 GeneticVariation CLINVAR

dbSNP: rs397516945
rs397516945
DSP
TA 0.700 GeneticVariation CLINVAR

dbSNP: rs397516955
rs397516955
DSP
A 0.700 GeneticVariation CLINVAR Desmosomal dysfunction due to mutations in desmoplakin causes arrhythmogenic right ventricular dysplasia/cardiomyopathy. 16917092

2006
dbSNP: rs397516955
rs397516955
DSP
A 0.700 GeneticVariation CLINVAR RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease. 25525159

2015
dbSNP: rs397516955
rs397516955
DSP
A 0.700 GeneticVariation CLINVAR The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing. 24503780

2014
dbSNP: rs397516956
rs397516956
DSP
CA 0.700 GeneticVariation CLINVAR Loss of desmoplakin isoform I causes early onset cardiomyopathy and heart failure in a Naxos-like syndrome. 16467215

2006
dbSNP: rs397516956
rs397516956
DSP
CA 0.700 GeneticVariation CLINVAR Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma. 11063735

2000
dbSNP: rs397516973
rs397516973
DSP
A 0.700 GeneticVariation CLINVAR Desmosomal dysfunction due to mutations in desmoplakin causes arrhythmogenic right ventricular dysplasia/cardiomyopathy. 16917092

2006
dbSNP: rs587782927
rs587782927
DSP
C 0.700 GeneticVariation CLINVAR

dbSNP: rs727502994
rs727502994
DSP
TAG 0.700 GeneticVariation CLINVAR

dbSNP: rs727503001
rs727503001
DSP
A 0.700 GeneticVariation CLINVAR

dbSNP: rs727503003
rs727503003
DSP
CA 0.700 GeneticVariation CLINVAR Familial evaluation in arrhythmogenic right ventricular cardiomyopathy: impact of genetics and revised task force criteria. 21606390

2011
dbSNP: rs727503003
rs727503003
DSP
CA 0.700 GeneticVariation CLINVAR Prevalence of desmosomal protein gene mutations in patients with dilated cardiomyopathy. 20716751

2010
dbSNP: rs727503003
rs727503003
DSP
CA 0.700 GeneticVariation CLINVAR Desmosomal protein gene mutations in patients with idiopathic dilated cardiomyopathy undergoing cardiac transplantation: a clinicopathological study. 21859740

2011
dbSNP: rs727504443
rs727504443
DSP
A 0.700 GeneticVariation CLINVAR Left-dominant arrhythmogenic cardiomyopathy: an under-recognized clinical entity. 19095136

2008
dbSNP: rs727504443
rs727504443
DSP
A 0.700 GeneticVariation CLINVAR The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing. 24503780

2014
dbSNP: rs727504443
rs727504443
DSP
A 0.700 GeneticVariation CLINVAR Wide spectrum of desmosomal mutations in Danish patients with arrhythmogenic right ventricular cardiomyopathy. 20864495

2010