ClinVar Miner

Submissions for variant NM_002972.4(SBF1):c.1333-4dup

gnomAD frequency: 0.00149  dbSNP: rs138346146
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002117802 SCV002402995 benign not provided 2024-01-11 criteria provided, single submitter clinical testing
GeneDx RCV002117802 SCV005327953 likely benign not provided 2024-02-27 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.

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