ClinVar Miner

Submissions for variant NM_001084.5(PLOD3):c.123G>A (p.Val41=)

gnomAD frequency: 0.00313  dbSNP: rs112321807
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000508101 SCV000604871 benign not provided 2017-11-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000508101 SCV001118763 benign not provided 2025-01-30 criteria provided, single submitter clinical testing

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