ClinVar Miner

Submissions for variant NM_017565.4(FAM20A):c.342C>T (p.Asp114=)

gnomAD frequency: 0.00006  dbSNP: rs778101746
Minimum review status: Collection method:
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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 RCV002106869 SCV002326813 likely benign not provided 2020-12-12 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002486802 SCV002801737 likely benign Amelogenesis imperfecta type 1G 2021-12-04 criteria provided, single submitter clinical testing

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