ClinVar Miner

Submissions for variant NM_017780.4(CHD7):c.3202-4dup

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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 RCV005136191 SCV005765421 likely benign CHARGE syndrome 2024-08-29 criteria provided, single submitter clinical testing

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