ClinVar Miner

Submissions for variant NM_020791.4(TAOK1):c.*3451T>A

dbSNP: rs2508365262
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center RCV002280030 SCV002568153 uncertain significance Developmental delay with or without intellectual impairment or behavioral abnormalities 2022-04-08 criteria provided, single submitter clinical testing PM2

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