Source: BEFREE ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61661343
rs61661343
LMNA
0.720 GeneticVariation BEFREE Primary skin fibroblasts from DCM patients carrying the most prevalent Finnish founder mutation (p.S143P) in <i>LMNA</i> were reprogrammed into hiPSCs and further differentiated into cardiomyocytes (CMs). 31208058

2019
dbSNP: rs61661343
rs61661343
LMNA
0.720 GeneticVariation BEFREE Screening for the lamin A/C gene and, particularly, the S143P mutation seems warranted when patients with DCM have conduction system disturbances. 15140538

2004