ClinVar Miner

Submissions for variant NM_017780.4(CHD7):c.5666-19T>C

dbSNP: rs1805474762
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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 RCV002110863 SCV002435365 likely benign CHARGE syndrome 2023-08-24 criteria provided, single submitter clinical testing

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