ClinVar Miner

Submissions for variant NM_002382.5(MAX):c.-152TG[8]

dbSNP: rs886050638
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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 RCV000374857 SCV000387956 uncertain significance Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004693176 SCV005191422 uncertain significance not provided criteria provided, single submitter not provided

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