ClinVar Miner

Submissions for variant NM_001370259.2(MEN1):c.1350+7G>A

dbSNP: rs2136099113
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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 RCV001490747 SCV001695318 likely benign Multiple endocrine neoplasia, type 1 2019-10-09 criteria provided, single submitter clinical testing

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