rs797044485, LMNA

N. diseases: 4
Disease: Progeria ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Progeria
CUI: C0033300
Disease: Progeria
0.700 CausalMutation CLINVAR A novel lamin A/C mutation in a Dutch family with premature atherosclerosis. 23659872 2013