Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1553265736
rs1553265736
LMNA
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		C 0.700 GeneticVariation CLINVAR

dbSNP: rs794728602
rs794728602
LMNA
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		A 0.700 GeneticVariation CLINVAR