ClinVar Miner

Submissions for variant NM_182943.3(PLOD2):c.861C>T (p.Val287=)

gnomAD frequency: 0.00010  dbSNP: rs573318217
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000893736 SCV001037691 benign not provided 2024-11-04 criteria provided, single submitter clinical testing
GeneDx RCV000893736 SCV001813223 likely benign not provided 2021-05-04 criteria provided, single submitter clinical testing

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