ClinVar Miner

Submissions for variant NM_001029.5(RPS26):c.181+19C>G

dbSNP: rs201040758
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002181072 SCV002473887 likely benign Diamond-Blackfan anemia 10 2024-01-06 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002181072 SCV002803439 likely benign Diamond-Blackfan anemia 10 2021-11-05 criteria provided, single submitter clinical testing

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