ClinVar Miner

Submissions for variant NM_003742.4(ABCB11):c.3828C>T (p.Arg1276=)

dbSNP: rs2105873738
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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 RCV001468083 SCV001672121 likely benign not provided 2020-06-23 criteria provided, single submitter clinical testing

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