ClinVar Miner

Submissions for variant NM_001029.5(RPS26):c.69C>T (p.Cys23=)

gnomAD frequency: 0.00001  dbSNP: rs986563758
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001413264 SCV001615375 likely benign Diamond-Blackfan anemia 10 2020-06-06 criteria provided, single submitter clinical testing

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