ClinVar Miner

Submissions for variant NM_020975.6(RET):c.*453G>T

dbSNP: rs886046993
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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 RCV000280125 SCV000362424 uncertain significance Hirschsprung Disease, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000337622 SCV000362425 uncertain significance Renal hypodysplasia/aplasia 1 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000375834 SCV000362426 uncertain significance Multiple endocrine neoplasia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000293193 SCV000362427 uncertain significance Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing

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