ClinVar Miner

Submissions for variant NM_001002010.5(NT5C3A):c.354+17A>G

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003613030 SCV004562476 likely benign Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency 2023-08-30 criteria provided, single submitter clinical testing

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