ClinVar Miner

Submissions for variant NM_000352.6(ABCC8):c.2695-20G>A

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003120209 SCV003800054 likely benign not provided 2022-03-23 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003491319 SCV004241241 likely benign not specified 2023-12-18 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003120209 SCV004353252 benign not provided 2024-01-29 criteria provided, single submitter clinical testing

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