ClinVar Miner

Submissions for variant NM_020975.6(RET):c.1834_1860del (p.Phe612_Cys620del)

dbSNP: rs121913313
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000420537 SCV000505638 likely pathogenic Medullary thyroid carcinoma 2015-07-14 no assertion criteria provided literature only

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