ClinVar Miner

Submissions for variant NM_001291303.3(FAT4):c.3150T>C (p.Gly1050=)

gnomAD frequency: 0.00002  dbSNP: rs1379648279
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003037559 SCV003322693 likely benign not provided 2023-10-17 criteria provided, single submitter clinical testing

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