ClinVar Miner

Submissions for variant NM_020975.6(RET):c.*388G>A (rs3026782)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000308196 SCV000362416 likely benign Hirschsprung Disease, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000365222 SCV000362417 likely benign Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000272787 SCV000362418 likely benign Renal adysplasia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000321083 SCV000362419 likely benign Multiple endocrine neoplasia 2016-06-14 criteria provided, single submitter clinical testing

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