ClinVar Miner

Submissions for variant NM_000392.5(ABCC2):c.1644C>T (p.Phe548=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003866303 SCV004669179 likely benign not provided 2023-10-22 criteria provided, single submitter clinical testing

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