rs57077886, LMNA

N. diseases: 9
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 A Novel Generalized Lipodystrophy-Associated Progeroid Syndrome Due to Recurrent Heterozygous LMNA p.T10I Mutation. 29267953 2018