ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.89568T>C (p.Asp29856=)

gnomAD frequency: 0.00002  dbSNP: rs759394282
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001424246 SCV001626840 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2024-05-04 criteria provided, single submitter clinical testing
Ambry Genetics RCV002368327 SCV002656390 likely benign Cardiovascular phenotype 2021-10-08 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
Breakthrough Genomics, Breakthrough Genomics RCV004711617 SCV005259388 likely benign not provided criteria provided, single submitter not provided

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