ClinVar Miner

Submissions for variant NM_017780.4(CHD7):c.5895-5A>T

dbSNP: rs1805499680
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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 RCV001216673 SCV001388481 likely benign CHARGE syndrome 2021-12-14 criteria provided, single submitter clinical testing

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