ClinVar Miner

Submissions for variant NM_003742.4(ABCB11):c.2088G>T (p.Arg696=)

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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 RCV002791923 SCV003201281 likely benign not provided 2022-05-21 criteria provided, single submitter clinical testing

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