ClinVar Miner

Submissions for variant NM_020975.6(RET):c.60G>C (p.Pro20=)

gnomAD frequency: 0.00001  dbSNP: rs1263991822
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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 RCV002179932 SCV002348450 likely benign Multiple endocrine neoplasia, type 2 2021-04-08 criteria provided, single submitter clinical testing

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