DisGeNET - a database of gene-disease associations

LMNB2, lamin B2, 84823

N. diseases: 74; N. variants: 3

Disease: Myoclonic Epilepsies, Progressive ×

Source: ALL

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Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _v

DPI _v

pLI

EI _vda

EL _gda

Score _vda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

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