ClinVar Miner

Submissions for variant NM_004260.4(RECQL4):c.118+18C>T

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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 RCV003615679 SCV004548457 likely benign Baller-Gerold syndrome 2023-03-19 criteria provided, single submitter clinical testing

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