ClinVar Miner

Submissions for variant NM_020975.6(RET):c.3017A>G (p.Glu1006Gly)

dbSNP: rs2538627588
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
All of Us Research Program, National Institutes of Health RCV004009902 SCV004817983 uncertain significance Multiple endocrine neoplasia, type 2 2023-03-04 criteria provided, single submitter clinical testing

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