ClinVar Miner

Submissions for variant NM_017565.4(FAM20A):c.404+18G>A

gnomAD frequency: 0.00011  dbSNP: rs773191671
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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 RCV002151841 SCV002462566 likely benign not provided 2024-12-31 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002500333 SCV002807371 likely benign Amelogenesis imperfecta type 1G 2021-07-23 criteria provided, single submitter clinical testing

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