ClinVar Miner

Submissions for variant NM_020975.6(RET):c.1649-11G>C

dbSNP: rs746325077
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002207980 SCV002375476 likely benign Multiple endocrine neoplasia, type 2 2022-01-27 criteria provided, single submitter clinical testing

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