ClinVar Miner

Submissions for variant NM_002230.4(JUP):c.1092C>T (p.Asn364=)

dbSNP: rs1555603222
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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 RCV002125288 SCV002449839 likely benign Naxos disease; Arrhythmogenic right ventricular dysplasia 12 2021-02-19 criteria provided, single submitter clinical testing
Ambry Genetics RCV004990696 SCV005601752 likely benign Cardiovascular phenotype 2024-10-28 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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