ClinVar Miner

Submissions for variant NM_004064.5(CDKN1B):c.476-10C>T

gnomAD frequency: 0.00001  dbSNP: rs200108977
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000864981 SCV001005875 likely benign Multiple endocrine neoplasia type 4 2024-01-22 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV000864981 SCV002797297 likely benign Multiple endocrine neoplasia type 4 2022-05-16 criteria provided, single submitter clinical testing

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