ClinVar Miner

Submissions for variant NM_001039591.3(USP9X):c.6360A>G (p.Ile2120Met)

gnomAD frequency: 0.00013  dbSNP: rs201128029
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV001093491 SCV001250511 uncertain significance not provided 2019-09-01 criteria provided, single submitter clinical testing
GeneDx RCV001093491 SCV002504378 likely benign not provided 2021-02-24 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.
Labcorp Genetics (formerly Invitae), Labcorp RCV001093491 SCV004299820 benign not provided 2024-01-22 criteria provided, single submitter clinical testing

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