ClinVar Miner

Submissions for variant NM_000244.3(MEN1):c.1095C>T (p.Ile365=) (rs147331514)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000988572 SCV000259317 likely benign Multiple endocrine neoplasia, type 1 2019-12-31 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000506264 SCV000604205 likely benign not specified 2016-09-12 criteria provided, single submitter clinical testing
Ambry Genetics RCV000574517 SCV000664496 likely benign Hereditary cancer-predisposing syndrome 2015-12-04 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign
Mendelics RCV000988572 SCV001138342 likely benign Multiple endocrine neoplasia, type 1 2019-05-28 criteria provided, single submitter clinical testing

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