ClinVar Miner

Submissions for variant NM_005245.4(FAT1):c.13359C>T (p.Pro4453=)

gnomAD frequency: 0.00218  dbSNP: rs147776400
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 RCV000881203 SCV001024358 benign not provided 2024-11-18 criteria provided, single submitter clinical testing
GeneDx RCV000881203 SCV001796855 likely benign not provided 2020-05-13 criteria provided, single submitter clinical testing

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