ClinVar Miner

Submissions for variant NM_020975.6(RET):c.1064-16G>T

gnomAD frequency: 0.00004  dbSNP: rs373327241
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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 RCV002179495 SCV002337448 likely benign Multiple endocrine neoplasia, type 2 2024-11-16 criteria provided, single submitter clinical testing

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