ClinVar Miner

Submissions for variant NM_000170.3(GLDC):c.2127C>T (p.Asn709=)

dbSNP: rs753895623
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001460889 SCV001664771 likely benign Non-ketotic hyperglycinemia 2020-04-06 criteria provided, single submitter clinical testing

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