ClinVar Miner

Submissions for variant NM_004260.4(RECQL4):c.3056-5G>T

dbSNP: rs774320251
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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 RCV002209516 SCV002366076 likely benign Baller-Gerold syndrome 2021-08-09 criteria provided, single submitter clinical testing

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