ClinVar Miner

Submissions for variant NM_024422.6(DSC2):c.155-1G>A

dbSNP: rs1987629887
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001178892 SCV001343456 uncertain significance Cardiomyopathy 2018-11-13 criteria provided, single submitter clinical testing This variant alters the canonical splice acceptor site in intron 2 of the DSC2 gene. Computational splicing tools predict that this variant may have significant adverse effects on splicing. To our knowledge, RNA study has not been performed to investigate the molecular impact of this variant. This variant has not been reported in individuals affected with cardiovascular disorders or in unaffected control individuals in the literature. This variant is rare in the general population and has been identified in 0/277264 chromosomes by the Genome Aggregation Database (gnomAD). Although this variant affects a canonical splice acceptor site, its molecular impact is not known and available evidence is insufficient to determine the role of this variant in disease conclusively. Therefore, this variant is classified as a Variant of Uncertain Significance.

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