ClinVar Miner

Submissions for variant NM_001122630.2(CDKN1C):c.842C>T (p.Pro281Leu)

dbSNP: rs1317648965
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital RCV002488695 SCV002775029 uncertain significance not provided 2022-12-17 criteria provided, single submitter clinical testing

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