ClinVar Miner

Submissions for variant NM_020975.6(RET):c.*509A>G

dbSNP: rs886046996
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000303593 SCV000362436 uncertain significance Renal hypodysplasia/aplasia 1 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000360823 SCV000362437 uncertain significance Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000268470 SCV000362438 uncertain significance Hirschsprung Disease, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000316349 SCV000362439 uncertain significance Multiple endocrine neoplasia 2016-06-14 criteria provided, single submitter clinical testing

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