ClinVar Miner

Submissions for variant NC_000022.10:g.(?_19743473)_(19929346_?)dup

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000628832 SCV000749739 uncertain significance Primary dilated cardiomyopathy 2018-03-27 criteria provided, single submitter clinical testing A gross duplication of the genomic region encompassing the full coding sequence of the TXNRD2 gene has been identified. The boundaries of this event are unknown as the duplication extends beyond the assayed region for this gene and therefore may encompass additional genes. As the precise location of this duplication is unknown, it may be in tandem or it may be located elsewhere in the genome. This variant has not been reported in the literature in individuals with TXNRD2-related disease. Experimental studies and prediction algorithms are not available for this variant, and the functional significance of the duplicated amino acid(s) is currently unknown. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

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