ClinVar Miner

Submissions for variant NM_004260.4(RECQL4):c.119-7C>T

dbSNP: rs2130741953
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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 RCV001425069 SCV001627680 likely benign Baller-Gerold syndrome 2020-09-14 criteria provided, single submitter clinical testing

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