ClinVar Miner

Submissions for variant NM_001371333.1(DIABLO):c.524-20A>C

gnomAD frequency: 0.00004  dbSNP: rs535135642
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001759279 SCV002004935 likely benign not provided 2021-02-17 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001759279 SCV002933257 benign not provided 2023-10-25 criteria provided, single submitter clinical testing

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