ClinVar Miner

Submissions for variant NM_001032.5(RPS29):c.163-4del

dbSNP: rs373877728
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001717427 SCV001944669 benign not provided 2020-01-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001717427 SCV002383416 benign not provided 2023-11-21 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002496040 SCV002801129 likely benign Diamond-Blackfan anemia 13 2022-01-13 criteria provided, single submitter clinical testing

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