ClinVar Miner

Submissions for variant NM_003742.4(ABCB11):c.3564C>G (p.Val1188=)

dbSNP: rs1574394077
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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 RCV001497744 SCV001702481 likely benign not provided 2022-07-19 criteria provided, single submitter clinical testing

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