ClinVar Miner

Submissions for variant NM_020975.6(RET):c.*1116T>C (rs2435355)

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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 RCV000260152 SCV000362484 likely benign Multiple endocrine neoplasia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000324757 SCV000362485 likely benign Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000379318 SCV000362486 likely benign Renal adysplasia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000284603 SCV000362487 likely benign Hirschsprung Disease, Dominant 2016-06-14 criteria provided, single submitter clinical testing

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