Gene: MYPN ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs140148105
rs140148105
MYPN
G 0.800 GeneticVariation CLINVAR Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations. 22286171

2012
dbSNP: rs71534278
rs71534278
MYPN
T 0.800 GeneticVariation CLINVAR Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations. 22286171

2012
dbSNP: rs140148105
rs140148105
MYPN
G 0.800 CausalMutation CLINVAR

dbSNP: rs71534278
rs71534278
MYPN
T 0.800 CausalMutation CLINVAR

dbSNP: rs71534280
rs71534280
MYPN
A 0.800 CausalMutation CLINVAR

dbSNP: rs864621995
rs864621995
MYPN
T 0.800 CausalMutation CLINVAR

dbSNP: rs865921466
rs865921466
MYPN
A 0.700 GeneticVariation CLINVAR