Gene: DSP ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121912998
rs121912998
DSP ; LOC101928076
A 0.700 CausalMutation CLINVAR Postmortem genetic screening for the identification, verification, and reporting of genetic variants contributing to the sudden death of the young. 27435932

2016
dbSNP: rs730880092
rs730880092
DSP
G 0.700 GeneticVariation CLINVAR Compound heterozygous desmoplakin mutations result in a phenotype with a combination of myocardial, skin, hair, and enamel abnormalities. 19924139

2010
dbSNP: rs1561686893
rs1561686893
DSP
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1561690319
rs1561690319
DSP
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1561698362
rs1561698362
DSP
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1561698714
rs1561698714
DSP
GA 0.700 GeneticVariation CLINVAR

dbSNP: rs1561701721
rs1561701721
DSP
TC 0.700 GeneticVariation CLINVAR

dbSNP: rs1561702549
rs1561702549
DSP
CT 0.700 GeneticVariation CLINVAR

dbSNP: rs193922668
rs193922668
DSP
C 0.700 GeneticVariation CLINVAR

dbSNP: rs193922671
rs193922671
DSP
G 0.700 GeneticVariation CLINVAR

dbSNP: rs28763965
rs28763965
DSP
T 0.700 GeneticVariation CLINVAR

dbSNP: rs397516915
rs397516915
DSP
T 0.700 GeneticVariation CLINVAR

dbSNP: rs397516915
rs397516915
DSP
T 0.700 CausalMutation CLINVAR

dbSNP: rs397516955
rs397516955
DSP
A 0.700 GeneticVariation CLINVAR