ClinVar Miner

Submissions for variant NM_003118.4(SPARC):c.*582G>C

gnomAD frequency: 0.44854  dbSNP: rs1054204
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV002277851 SCV002565043 benign Osteogenesis imperfecta 2022-05-21 criteria provided, single submitter clinical testing

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