ClinVar Miner

Submissions for variant NM_024529.5(CDC73):c.-9G>C

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV003441346 SCV004167697 uncertain significance not provided 2023-04-12 criteria provided, single submitter clinical testing Nucleotide substitution has no predicted effect on splicing and is not conserved across species; Has not been previously published as pathogenic or benign to our knowledge

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