rs150840924, LMNA

N. diseases: 7
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Scleroderma
CUI: C0011644
Disease: Scleroderma
0.010 GeneticVariation BEFREE Progeroid syndrome with scleroderma-like skin changes associated with homozygous R435C LMNA mutation. 19842191 2009