ClinVar Miner

Submissions for variant NM_020975.6(RET):c.3162C>G (p.Ser1054=)

dbSNP: rs2133037102
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 RCV001394769 SCV001596459 likely benign Multiple endocrine neoplasia, type 2 2020-08-27 criteria provided, single submitter clinical testing

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