ClinVar Miner

Submissions for variant NM_020975.6(RET):c.*1599G>A (rs145954635)

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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 RCV000310427 SCV000362536 likely benign Hirschsprung Disease, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000364996 SCV000362537 likely benign Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000390291 SCV000362538 likely benign Renal adysplasia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000307007 SCV000362539 likely benign Multiple endocrine neoplasia 2016-06-14 criteria provided, single submitter clinical testing

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