ClinVar Miner

Submissions for variant NM_001291303.3(FAT4):c.9828C>T (p.Pro3276=)

gnomAD frequency: 0.00106  dbSNP: rs73849226
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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 RCV000903413 SCV000527336 likely benign not provided 2020-10-24 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000903413 SCV001047879 benign not provided 2025-01-23 criteria provided, single submitter clinical testing

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