ClinVar Miner

Submissions for variant NM_014324.6(AMACR):c.*976G>A

gnomAD frequency: 0.00754  dbSNP: rs150664086
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
Illumina Laboratory Services, Illumina RCV000381706 SCV000457111 likely benign Alpha-methylacyl-CoA racemase deficiency 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004711006 SCV005259742 likely benign not provided criteria provided, single submitter not provided

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