ClinVar Miner

Submissions for variant NM_020975.6(RET):c.1264-9C>T

gnomAD frequency: 0.00002  dbSNP: rs886636715
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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 RCV001436386 SCV001639228 likely benign Multiple endocrine neoplasia, type 2 2024-01-03 criteria provided, single submitter clinical testing

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