ClinVar Miner

Submissions for variant NM_003742.4(ABCB11):c.51T>C (p.Asn17=)

dbSNP: rs2106058394
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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 RCV002172213 SCV002334386 likely benign not provided 2021-03-13 criteria provided, single submitter clinical testing

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