ClinVar Miner

Submissions for variant NM_020975.6(RET):c.1522+16A>G

dbSNP: rs1588871514
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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 RCV003646461 SCV004430876 likely benign Multiple endocrine neoplasia, type 2 2023-02-09 criteria provided, single submitter clinical testing

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