Gene: LMNA ×
Source: INFERRED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397517906
rs397517906
LMNA
T 0.700 GeneticVariation CLINVAR Heart failure in patients with arrhythmogenic right ventricular cardiomyopathy: Genetic characteristics. 30765282

2019
dbSNP: rs397517906
rs397517906
LMNA
T 0.700 GeneticVariation CLINVAR Lamin mutation location predicts cardiac phenotype severity: combined analysis of the published literature. 30402260

2018
dbSNP: rs267607560
rs267607560
LMNA
T 0.700 GeneticVariation CLINVAR

dbSNP: rs57730570
rs57730570
LMNA
T 0.700 GeneticVariation CLINVAR

dbSNP: rs57730570
rs57730570
LMNA
A 0.700 CausalMutation CLINVAR

dbSNP: rs61094188
rs61094188
LMNA
T 0.700 GeneticVariation CLINVAR

dbSNP: rs794728588
rs794728588
LMNA
T 0.700 GeneticVariation CLINVAR