ClinVar Miner

Submissions for variant NM_001291303.3(FAT4):c.10107A>G (p.Glu3369=)

gnomAD frequency: 0.00140  dbSNP: rs147646369
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000908163 SCV000718643 likely benign not provided 2021-06-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000908163 SCV001052910 benign not provided 2024-01-25 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV000908163 SCV001929372 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000908163 SCV001963979 likely benign not provided no assertion criteria provided clinical testing

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