ClinVar Miner

Submissions for variant NM_020975.6(RET):c.2730+13G>A

gnomAD frequency: 0.00001  dbSNP: rs371761256
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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 RCV002219070 SCV002378153 likely benign Multiple endocrine neoplasia, type 2 2024-09-28 criteria provided, single submitter clinical testing

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