Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs57077886
rs57077886
LMNA
CUI: C0009207
Disease: Cockayne Syndrome
Cockayne Syndrome 		0.010 GeneticVariation BEFREE A Novel Generalized Lipodystrophy-Associated Progeroid Syndrome Due to Recurrent Heterozygous LMNA p.T10I Mutation. 29267953

2018