ClinVar Miner

Submissions for variant NM_000398.7(CYB5R3):c.890G>A (p.Arg297His) (rs76458556)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Kariminejad - Najmabadi Pathology & Genetics Center RCV000856706 SCV000999243 uncertain significance Neurodevelopmental delay 2018-09-22 criteria provided, single submitter clinical testing
Invitae RCV000949631 SCV001095895 likely benign not provided 2019-12-31 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV001000219 SCV001156736 uncertain significance none provided 2020-08-07 criteria provided, single submitter clinical testing

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