ClinVar Miner

Submissions for variant NM_020975.6(RET):c.1648+7C>T

dbSNP: rs1588872274
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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 RCV001470975 SCV001675075 likely benign Multiple endocrine neoplasia, type 2 2020-03-08 criteria provided, single submitter clinical testing

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