ClinVar Miner

Submissions for variant NM_017780.4(CHD7):c.3600C>T (p.Pro1200=)

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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 RCV003046117 SCV003323957 benign CHARGE syndrome 2022-09-19 criteria provided, single submitter clinical testing

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