ClinVar Miner

Submissions for variant NM_017780.4(CHD7):c.2745C>T (p.Asp915=)

dbSNP: rs1586389389
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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 RCV000910053 SCV001054896 likely benign not provided 2018-01-19 criteria provided, single submitter clinical testing

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