ClinVar Miner

Submissions for variant NM_003922.4(HERC1):c.4464-25_4464-24dup

dbSNP: rs369792267
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001552517 SCV001773219 likely benign not provided 2020-01-12 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001552517 SCV002390813 benign not provided 2025-01-06 criteria provided, single submitter clinical testing

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