ClinVar Miner

Submissions for variant NM_001370259.2(MEN1):c.784-16C>T

gnomAD frequency: 0.00002  dbSNP: rs754257177
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000662550 SCV000785133 likely benign Multiple endocrine neoplasia, type 1 2017-05-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000662550 SCV002392950 likely benign Multiple endocrine neoplasia, type 1 2024-09-02 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV000662550 SCV004018044 likely benign Multiple endocrine neoplasia, type 1 2023-04-17 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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