ClinVar Miner

Submissions for variant NM_002541.4(OGDH):c.936-7G>A

gnomAD frequency: 0.00209  dbSNP: rs116644435
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001513977 SCV001721698 benign Oxoglutaricaciduria 2021-03-26 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000676717 SCV004156855 likely benign not provided 2022-05-01 criteria provided, single submitter clinical testing OGDH: BP4
Mayo Clinic Laboratories, Mayo Clinic RCV000676717 SCV000802517 likely benign not provided 2016-02-25 no assertion criteria provided clinical testing

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