ClinVar Miner

Submissions for variant NM_017565.4(FAM20A):c.444C>T (p.Ser148=)

gnomAD frequency: 0.00235  dbSNP: rs139743735
Minimum review status: Collection method:
Minimum conflict level:
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 RCV000889116 SCV001032778 benign not provided 2023-12-26 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002479015 SCV002797856 benign Amelogenesis imperfecta type 1G 2021-08-16 criteria provided, single submitter clinical testing

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