ClinVar Miner

Submissions for variant NM_020223.4(FAM20C):c.1505+13C>A

gnomAD frequency: 0.00807  dbSNP: rs143984648
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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 RCV001513362 SCV001720965 benign not provided 2024-01-15 criteria provided, single submitter clinical testing
GeneDx RCV001513362 SCV002575862 likely benign not provided 2021-05-25 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.

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