ClinVar Miner

Submissions for variant NM_020975.6(RET):c.1063+10G>A

gnomAD frequency: 0.00001  dbSNP: rs374666249
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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 RCV001428200 SCV001630895 likely benign Multiple endocrine neoplasia, type 2 2024-12-04 criteria provided, single submitter clinical testing

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