ClinVar Miner

Submissions for variant NM_000443.4(ABCB4):c.2478+40A>G

gnomAD frequency: 0.10700  dbSNP: rs7788404
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 RCV001717006 SCV001944318 benign not provided 2018-06-29 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001717006 SCV005273735 benign not provided criteria provided, single submitter not provided

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