ClinVar Miner

Submissions for variant NM_002382.5(MAX):c.*405G>A

gnomAD frequency: 0.00825  dbSNP: rs45440292
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000272704 SCV000387931 likely benign Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004703667 SCV005219476 likely benign not provided criteria provided, single submitter not provided

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