ClinVar Miner

Submissions for variant NM_004064.5(CDKN1B):c.475+9C>T

gnomAD frequency: 0.00001  dbSNP: rs1431449120
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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 RCV001428422 SCV001631120 likely benign Multiple endocrine neoplasia type 4 2020-10-01 criteria provided, single submitter clinical testing

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