ClinVar Miner

Submissions for variant NM_020975.6(RET):c.*763C>T

dbSNP: rs886047001
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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 RCV000369398 SCV000362460 uncertain significance Hirschsprung Disease, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000277277 SCV000362461 uncertain significance Renal hypodysplasia/aplasia 1 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000325309 SCV000362462 uncertain significance Multiple endocrine neoplasia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000382566 SCV000362463 uncertain significance Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing

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