ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.27298G>C (p.Ala9100Pro)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV005000857 SCV005621196 uncertain significance not provided 2024-03-08 criteria provided, single submitter clinical testing Available data are insufficient to determine the clinical significance of the variant at this time. This variant has not been reported in large, multi-ethnic general populations. (http://gnomad.broadinstitute.org) Computational tools predict that this variant is not damaging.

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