ClinVar Miner

Submissions for variant NM_020975.6(RET):c.963G>A (p.Gly321=)

dbSNP: rs1837780326
Minimum review status: Collection method:
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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 RCV001442723 SCV001645676 likely benign Multiple endocrine neoplasia, type 2 2022-10-13 criteria provided, single submitter clinical testing

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