ClinVar Miner

Submissions for variant NM_152783.5(D2HGDH):c.1307-24A>G (rs6756901)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Nilou-Genome Lab RCV001657832 SCV001876519 benign D-2-hydroxyglutaric aciduria 1 2021-07-30 criteria provided, single submitter clinical testing
GeneDx RCV001689681 SCV001910505 benign not provided 2021-05-11 criteria provided, single submitter clinical testing
Genetic Services Laboratory,University of Chicago RCV000145792 SCV000192929 likely benign not specified no assertion criteria provided clinical testing

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