ClinVar Miner

Submissions for variant NM_004821.3(HAND1):c.609C>G (p.Gly203=)

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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 RCV002582139 SCV003492152 likely benign Hypoplastic left heart syndrome 2023-11-27 criteria provided, single submitter clinical testing

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