ClinVar Miner

Submissions for variant NM_001291303.3(FAT4):c.2322C>T (p.Pro774=)

gnomAD frequency: 0.00016  dbSNP: rs200593370
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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
GeneDx RCV000840252 SCV000982174 likely benign not provided 2021-03-30 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000840252 SCV001078556 benign not provided 2024-10-30 criteria provided, single submitter clinical testing

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