ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.92226G>A (p.Arg30742=)

gnomAD frequency: 0.00001  dbSNP: rs759484932
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV000517830 SCV000616176 uncertain significance not specified 2017-01-31 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001506182 SCV001711100 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2024-09-15 criteria provided, single submitter clinical testing
Ambry Genetics RCV004023530 SCV005020799 likely benign Cardiovascular phenotype 2023-11-26 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.

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