ClinVar Miner

Submissions for variant NM_001370259.2(MEN1):c.972G>C (p.Leu324=)

dbSNP: rs1592643568
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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 RCV001446383 SCV001649429 likely benign Multiple endocrine neoplasia, type 1 2019-11-27 criteria provided, single submitter clinical testing

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