ClinVar Miner

Submissions for variant NM_004260.4(RECQL4):c.84+17G>T

dbSNP: rs794726914
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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 RCV001931594 SCV002204772 likely benign Baller-Gerold syndrome 2023-10-20 criteria provided, single submitter clinical testing

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