ClinVar Miner

Submissions for variant NM_003098.3(SNTA1):c.213C>G (p.Gly71=)

dbSNP: rs1374381593
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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 RCV001415643 SCV001617804 likely benign Long QT syndrome 2023-07-18 criteria provided, single submitter clinical testing
Ambry Genetics RCV002431865 SCV002729103 likely benign Cardiovascular phenotype 2020-03-06 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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