Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs797044487
rs797044487
LMNA
CUI: C0033300
Disease: Progeria
Progeria 		A 0.700 CausalMutation CLINVAR Coronary artery disease in a Werner syndrome-like form of progeria characterized by low levels of progerin, a splice variant of lamin A. 22065502

2011