rs540123967

This variant is located in the LMNB1 gene.

ClinVar annotation

Benign☆☆☆
2 submitters1 publication

not provided; LMNB1-related disorder

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About LMNB1

This gene encodes one of the two B-type lamin proteins and is a component of the nuclear lamina. A duplication of this gene is associated with autosomal dominant adult-onset leukodystrophy (ADLD). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]

View all LMNB1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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