ClinVar Miner

Submissions for variant NM_017565.4(FAM20A):c.640+11T>C

gnomAD frequency: 0.02884  dbSNP: rs8071830
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001637689 SCV001852681 benign not provided 2021-05-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001637689 SCV002388244 benign not provided 2025-01-29 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002488442 SCV002796038 likely benign Amelogenesis imperfecta type 1G 2021-10-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001637689 SCV005255663 benign not provided criteria provided, single submitter not provided

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