ClinVar Miner

Submissions for variant NM_000443.4(ABCB4):c.3486+10dup

dbSNP: rs8187809
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000348201 SCV000332921 benign not specified 2015-07-24 criteria provided, single submitter clinical testing
GeneDx RCV001537837 SCV000567840 likely benign not provided 2018-05-02 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 23684896)
Labcorp Genetics (formerly Invitae), Labcorp RCV001537837 SCV002377828 benign not provided 2025-02-02 criteria provided, single submitter clinical testing

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