ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.97887A>T (p.Gly32629=)

dbSNP: rs755894229
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001436094 SCV001638929 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2022-12-13 criteria provided, single submitter clinical testing
GeneDx RCV003159209 SCV003853055 likely benign not provided 2020-09-18 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.

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