ClinVar Miner

Submissions for variant NM_004064.5(CDKN1B):c.12G>A (p.Val4=)

dbSNP: rs1555085477
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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 RCV000645527 SCV000767273 likely benign Multiple endocrine neoplasia type 4 2017-10-27 criteria provided, single submitter clinical testing

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