ClinVar Miner

Submissions for variant NM_004960.4(FUS):c.1542-5dup

dbSNP: rs371057360
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001565413 SCV001788752 likely benign not provided 2020-08-14 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001565413 SCV001809062 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV001701196 SCV001923966 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001701196 SCV001931880 benign not specified no assertion criteria provided clinical testing

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