ClinVar Miner

Submissions for variant NM_001370259.2(MEN1):c.1056C>T (p.Asn352=)

dbSNP: rs1565642741
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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 RCV001417821 SCV001620027 likely benign Multiple endocrine neoplasia, type 1 2020-10-15 criteria provided, single submitter clinical testing

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