ClinVar Miner

Submissions for variant NM_000363.5(TNNI3):c.549+68_549+69insGGCCTA (rs139158921)

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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 RCV000030564 SCV000053235 uncertain Primary familial hypertrophic cardiomyopathy 2011-08-18 criteria provided, single submitter curation Converted during submission to Uncertain significance.

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