ClinVar Miner

Submissions for variant NM_001370259.2(MEN1):c.42C>G (p.Arg14=)

dbSNP: rs765446407
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001416376 SCV001618556 likely benign Multiple endocrine neoplasia, type 1 2019-09-21 criteria provided, single submitter clinical testing

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