ClinVar Miner

Submissions for variant NC_000001.10:g.(?_12020693)_(12027158_?)dup

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000800656 SCV000940386 pathogenic Ehlers-Danlos syndrome, kyphoscoliotic type 1 2019-10-08 criteria provided, single submitter clinical testing This variant is a gross duplication of the genomic region encompassing exons 10-16 of the PLOD1 gene. While the exact position of the duplicated exons cannot be determined from this data, the duplicated copy of this region is likely in tandem and in-frame, therefore preserving the integrity of the reading frame. Duplications encompassing exons 10-16 have been reported in the homozygous state or in trans with a pathogenic variant in several individuals affected with Ehlers-Danlos syndrome (PMID: 7977351, 8981946, 19320026, 25277362). In a screening of 291 control individuals from the U.S, this variant was only found in one allele (PMID: 8981946). Experimental studies and prediction algorithms are not available for this variant, and the functional significance of the duplicated exons is currently unknown. For these reasons, this variant has been classified as Pathogenic.

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