ClinVar Miner

Submissions for variant NM_003742.4(ABCB11):c.372A>T (p.Thr124=)

dbSNP: rs2106047515
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002183602 SCV002480318 likely benign not provided 2020-12-10 criteria provided, single submitter clinical testing

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