ClinVar Miner

Submissions for variant NM_000033.4(ABCD1):c.320T>C (p.Leu107Pro) (rs1569540688)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Consultorio y Laboratorio de Neurogenética,Hospital JM Ramos Mejia RCV000722143 SCV000845208 likely pathogenic Adrenoleukodystrophy 2018-10-29 criteria provided, single submitter research Abnormalities of the ABCD1 gene have been frequently identified as the underlying cause of adrenoleukodystrophy (ALD), a demyelinating disorder of the recessively inherited nervous system of the X chromosome. For the first time, in 1996, Krasemann et al. reported the presence of variants in this gene in 20 families affected with ALD. We are the first to report and argue that due to its location within a coding region this variant in ABCD1 of a patient diagnosed with ALD has functional consequences. The large number of reports available in the literature associate the presence of variants in this gene with ALD.
Institute of Human Genetics, University of Leipzig Medical Center RCV000722143 SCV001429298 likely pathogenic Adrenoleukodystrophy 2019-05-28 criteria provided, single submitter clinical testing This variant was identified as hemizygous

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