ClinVar Miner

Submissions for variant NM_000435.3(NOTCH3):c.2300G>A (p.Arg767His) (rs75291244)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000247799 SCV000304249 benign not specified criteria provided, single submitter clinical testing
Invitae RCV000871017 SCV001012612 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV000247799 SCV001159879 likely benign not specified 2019-05-08 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000247799 SCV001879586 benign not specified 2020-11-16 criteria provided, single submitter clinical testing

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