ClinVar Miner

Submissions for variant NM_003742.4(ABCB11):c.1512G>A (p.Glu504=)

dbSNP: rs1486107533
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 RCV001437991 SCV001640857 likely benign not provided 2022-10-03 criteria provided, single submitter clinical testing

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