ClinVar Miner

Submissions for variant NM_024741.3(ZNF408):c.581_592del (p.Val194_Val197del)

dbSNP: rs148055528
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000248955 SCV000314391 benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000948864 SCV001095090 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
GeneDx RCV000948864 SCV001910670 benign not provided 2021-05-05 criteria provided, single submitter clinical testing
Dept Of Ophthalmology, Nagoya University RCV003888664 SCV004706957 benign Retinal dystrophy 2023-10-01 criteria provided, single submitter research
Institute of Human Genetics, Univ. Regensburg, Univ. Regensburg RCV003888664 SCV005070138 uncertain significance Retinal dystrophy 2022-01-01 no assertion criteria provided clinical testing

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