LMNA, lamin A/C, 4000

N. diseases: 824; N. variants: 285
Disease: Progeria Syndrome, Childhood-Onset ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs60652225
rs60652225
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
CUI: C2750285
Disease:
Progeria Syndrome, Childhood-Onset 		G 0.700 CausalMutation CLINVAR
dbSNP: rs60864230
rs60864230
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
CUI: C2750285
Disease:
Progeria Syndrome, Childhood-Onset 		T 0.700 CausalMutation CLINVAR
dbSNP: rs730882262
rs730882262
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
CUI: C2750285
Disease:
Progeria Syndrome, Childhood-Onset 		G 0.700 CausalMutation CLINVAR