ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.71266G>A (p.Gly23756Ser)

dbSNP: rs2468650185
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003143009 SCV003822211 uncertain significance not provided 2020-05-05 criteria provided, single submitter clinical testing
New York Genome Center RCV003336821 SCV004046626 uncertain significance Dilated cardiomyopathy 1G; Hypertrophic cardiomyopathy 9 2022-12-08 criteria provided, single submitter clinical testing

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