ClinVar Miner

Submissions for variant NM_004260.4(RECQL4):c.1131+11G>A

dbSNP: rs369167534
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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 RCV002097960 SCV002388340 likely benign Baller-Gerold syndrome 2025-01-13 criteria provided, single submitter clinical testing

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