ClinVar Miner

Submissions for variant NM_017565.4(FAM20A):c.321G>C (p.Pro107=)

gnomAD frequency: 0.00007  dbSNP: rs568029338
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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 RCV000967461 SCV001114846 likely benign not provided 2022-12-29 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002488055 SCV002798082 likely benign Amelogenesis imperfecta type 1G 2022-02-15 criteria provided, single submitter clinical testing

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