ClinVar Miner

Submissions for variant NM_003470.3(USP7):c.807T>C (p.His269=)

gnomAD frequency: 0.00153  dbSNP: rs139232336
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
CeGaT Center for Human Genetics Tuebingen RCV001726984 SCV001961570 likely benign not provided 2024-07-01 criteria provided, single submitter clinical testing USP7: BP4, BP7, BS1
Labcorp Genetics (formerly Invitae), Labcorp RCV001726984 SCV003252034 benign not provided 2023-12-19 criteria provided, single submitter clinical testing

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