ClinVar Miner

Submissions for variant NM_014846.4(WASHC5):c.*3del

gnomAD frequency: 0.00146  dbSNP: rs569426560
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000205252 SCV000259915 benign Spastic paraplegia 2015-08-13 criteria provided, single submitter clinical testing
GeneDx RCV001571497 SCV001795982 likely benign not provided 2020-02-18 criteria provided, single submitter clinical testing
Athena Diagnostics RCV001657992 SCV001880458 benign not specified 2020-10-19 criteria provided, single submitter clinical testing

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