ClinVar Miner

Submissions for variant NM_003742.4(ABCB11):c.1268A>G (p.His423Arg)

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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 RCV002927742 SCV003263944 likely benign not provided 2024-03-19 criteria provided, single submitter clinical testing

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