ClinVar Miner

Submissions for variant NM_153717.3(EVC):c.153_174+42del

dbSNP: rs1723019796
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001210514 SCV001382005 likely pathogenic Ellis-van Creveld syndrome; Curry-Hall syndrome 2022-02-10 criteria provided, single submitter clinical testing This variant is not present in population databases (gnomAD no frequency). This variant results in the deletion of part of exon 1 (c.153_174+42del) of the EVC gene. It is expected to disrupt RNA splicing. Variants that disrupt the donor or acceptor splice site typically lead to a loss of protein function (PMID: 16199547), and loss-of-function variants in EVC are known to be pathogenic (PMID: 23220543). This variant has not been reported in the literature in individuals affected with EVC-related conditions. In summary, the currently available evidence indicates that the variant is pathogenic, but additional data are needed to prove that conclusively. Therefore, this variant has been classified as Likely Pathogenic. ClinVar contains an entry for this variant (Variation ID: 940843).

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