ClinVar Miner

Submissions for variant NM_001370259.2(MEN1):c.446-17A>G

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003030151 SCV003330788 likely benign Multiple endocrine neoplasia, type 1 2022-09-22 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV003030151 SCV005899755 likely benign Multiple endocrine neoplasia, type 1 2024-11-01 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.

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