ClinVar Miner

Submissions for variant NM_001039591.3(USP9X):c.6267T>C (p.Ala2089=)

gnomAD frequency: 0.00001  dbSNP: rs746438922
Minimum review status: Collection method:
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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 RCV001546933 SCV001766538 likely benign not provided 2020-06-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001546933 SCV003020614 likely benign not provided 2024-08-23 criteria provided, single submitter clinical testing

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