rs150840924, LMNA

N. diseases: 7
Disease: Cockayne Syndrome ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Cockayne Syndrome
CUI: C0009207
Disease: Cockayne Syndrome
0.010 GeneticVariation BEFREE Progeroid syndrome with scleroderma-like skin changes associated with homozygous R435C LMNA mutation. 19842191 2009