ClinVar Miner

Submissions for variant NM_030631.4(SLC25A21):c.270+15C>T

gnomAD frequency: 0.22479  dbSNP: rs10135196
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001807622 SCV002055902 benign Mitochondrial DNA depletion syndrome 18 2021-07-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002074218 SCV002401290 benign not provided 2024-02-01 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002074218 SCV005294185 benign not provided criteria provided, single submitter not provided

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