LMNA, lamin A/C, 4000

N. diseases: 824; N. variants: 285
Disease: Atrial Fibrillation ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28933093
rs28933093
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
CUI: C0004238
Disease:
Atrial Fibrillation 		0.010 GeneticVariation BEFREE A new missense (E161K) mutation was identified in a family with early atrial fibrillation and a previously described (R377H) mutation in another family with a quadriceps myopathy associated with DCM. 12920062 2003