LMNA, lamin A/C, 4000

N. diseases: 824; N. variants: 285
Disease: Malouf syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28928903
rs28928903
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
CUI: C0796031
Disease:
Malouf syndrome 		0.800 GeneticVariation UNIPROT
dbSNP: rs28928903
rs28928903
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
CUI: C0796031
Disease:
Malouf syndrome 		C 0.800 CausalMutation CLINVAR