ClinVar Miner

Submissions for variant NM_020975.6(RET):c.1086C>G (p.Leu362=)

dbSNP: rs2132743034
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 RCV002208315 SCV002494630 likely benign Multiple endocrine neoplasia, type 2 2021-01-28 criteria provided, single submitter clinical testing

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