ClinVar Miner

Submissions for variant NM_002972.4(SBF1):c.1432-13C>T

gnomAD frequency: 0.00021  dbSNP: rs76515527
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001556372 SCV001777942 likely benign not provided 2020-07-28 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001556372 SCV002352618 benign not provided 2024-01-15 criteria provided, single submitter clinical testing

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