ClinVar Miner

Submissions for variant NM_020975.6(RET):c.1617C>G (p.Gly539=)

dbSNP: rs1554818648
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000654628 SCV000776522 likely benign Multiple endocrine neoplasia, type 2 2024-02-18 criteria provided, single submitter clinical testing

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