ClinVar Miner

Submissions for variant NM_003742.4(ABCB11):c.1809+86G>A

gnomAD frequency: 0.03876  dbSNP: rs7576531
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001719620 SCV001948884 benign not provided 2018-11-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001719620 SCV005244735 benign not provided criteria provided, single submitter not provided

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