ClinVar Miner

Submissions for variant NM_000038.6(APC):c.8465G>C (p.Ser2822Thr)

dbSNP: rs1421264825
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000757003 SCV000885024 uncertain significance not provided 2017-10-31 criteria provided, single submitter clinical testing

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