ClinVar Miner

Submissions for variant NM_020975.6(RET):c.1420C>T (p.Arg474Trp) (rs775842917)

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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 RCV000402202 SCV000362303 uncertain significance Renal adysplasia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000292520 SCV000362304 uncertain significance Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000352045 SCV000362305 uncertain significance Hirschsprung Disease, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000390089 SCV000362306 uncertain significance Multiple endocrine neoplasia 2016-06-14 criteria provided, single submitter clinical testing

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