ClinVar Miner

Submissions for variant NM_002230.4(JUP):c.1105G>T (p.Val369Leu)

dbSNP: rs1915425116
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV001328933 SCV001520180 uncertain significance Arrhythmogenic right ventricular dysplasia 12 2020-07-28 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].

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