ClinVar Miner

Submissions for variant NM_003849.4(SUCLG1):c.458T>A (p.Val153Glu)

dbSNP: rs1573369925
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV002246752 SCV002519830 pathogenic Mitochondrial DNA depletion syndrome 9 2022-05-04 criteria provided, single submitter clinical testing

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