ClinVar Miner

Submissions for variant NM_002382.5(MAX):c.-126AGTG[4]

dbSNP: rs556734672
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000354961 SCV000387953 likely benign Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing
Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden RCV002262984 SCV002010475 uncertain significance not provided 2021-11-03 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002262984 SCV002545184 benign not provided 2023-07-01 criteria provided, single submitter clinical testing MAX: BS1, BS2

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