ClinVar Miner

Submissions for variant NM_017565.4(FAM20A):c.18G>A (p.Arg6=)

gnomAD frequency: 0.01179  dbSNP: rs75228334
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000961518 SCV001108566 benign not provided 2025-01-19 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002503007 SCV002801569 likely benign Amelogenesis imperfecta type 1G 2021-09-28 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000961518 SCV005255670 benign not provided criteria provided, single submitter not provided

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