ClinVar Miner

Submissions for variant NM_012309.5(SHANK2):c.2531T>C (p.Met844Thr)

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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 RCV003615815 SCV004565324 uncertain significance Autism, susceptibility to, 17 2023-09-11 criteria provided, single submitter clinical testing

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