ClinVar Miner

Submissions for variant NM_020223.4(FAM20C):c.1464C>T (p.His488=)

gnomAD frequency: 0.01913  dbSNP: rs139144760
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001514239 SCV001722039 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
GeneDx RCV001514239 SCV001867974 benign not provided 2021-05-04 criteria provided, single submitter clinical testing

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