ClinVar Miner

Submissions for variant NM_000102.4(CYP17A1):c.330G>A (p.Lys110=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV005164085 SCV005790688 likely benign not provided 2024-02-09 criteria provided, single submitter clinical testing

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