ClinVar Miner

Submissions for variant NM_001099271.2(POC5):c.1272C>T (p.Val424=)

dbSNP: rs35898774
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 RCV002210562 SCV002494443 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002210562 SCV005302208 benign not provided criteria provided, single submitter not provided

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