ClinVar Miner

Submissions for variant NM_003742.4(ABCB11):c.3407A>G (p.Lys1136Arg)

gnomAD frequency: 0.00006  dbSNP: rs752974260
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV002266379 SCV002548290 uncertain significance not specified 2022-05-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003096030 SCV003456937 likely benign not provided 2024-11-04 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV003096030 SCV004238845 uncertain significance not provided 2023-11-01 criteria provided, single submitter clinical testing

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