ClinVar Miner

Submissions for variant NM_001084.5(PLOD3):c.2061+12T>C

gnomAD frequency: 0.19416  dbSNP: rs4729671
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001710052 SCV001937930 benign not provided 2018-09-06 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001710052 SCV002489699 benign not provided 2025-02-04 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001710052 SCV005268256 benign not provided criteria provided, single submitter not provided

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