ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.24898G>C (p.Glu8300Gln)

dbSNP: rs1300968279
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV002266147 SCV002547655 uncertain significance not specified 2022-05-23 criteria provided, single submitter clinical testing

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