ClinVar Miner

Submissions for variant NC_000008.11:g.31059257_31099267del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001236493 SCV001409218 likely pathogenic Werner syndrome 2019-11-13 criteria provided, single submitter clinical testing This variant results in the deletion of exons 4-17 and part of exon 3 (c.201_1982-1582delinsT) of the WRN gene. It is expected to disrupt RNA splicing and likely results in an absent or disrupted protein product. This variant has not been reported in the literature in individuals with WRN-related conditions. Loss-of-function variants in WRN are known to be pathogenic (PMID: 16673358). 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.

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