ClinVar Miner

Submissions for variant NM_020975.6(RET):c.*553G>T

dbSNP: rs886046998
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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 RCV000294156 SCV000362444 uncertain significance Multiple endocrine neoplasia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000332648 SCV000362445 uncertain significance Hirschsprung Disease, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000389582 SCV000362446 uncertain significance Renal hypodysplasia/aplasia 1 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000288950 SCV000362447 uncertain significance Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing

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