ClinVar Miner

Submissions for variant NM_003922.4(HERC1):c.4464-15G>T

dbSNP: rs116375944
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001794778 SCV002032740 likely benign not provided 2021-06-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001794778 SCV002407997 benign not provided 2024-12-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001794778 SCV005215072 likely benign not provided criteria provided, single submitter not provided

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