ClinVar Miner

Submissions for variant NM_015102.5(NPHP4):c.2812G>A (p.Val938Met) (rs184961418)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000250885 SCV000312379 benign not specified criteria provided, single submitter clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000250885 SCV000331023 benign not specified 2015-12-09 criteria provided, single submitter clinical testing
Invitae RCV000533656 SCV000636141 benign Nephronophthisis 2019-12-31 criteria provided, single submitter clinical testing

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