ClinVar Miner

Submissions for variant NM_015971.4(MRPS7):c.83+23_83+24del

dbSNP: rs36039201
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001674993 SCV001886741 benign not provided 2018-06-28 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001776277 SCV002014260 benign Combined oxidative phosphorylation deficiency 34 2021-09-05 criteria provided, single submitter clinical testing

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