ClinVar Miner

Submissions for variant NM_020433.5(JPH2):c.1428G>A (p.Glu476=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV005189049 SCV005847669 likely benign Hypertrophic cardiomyopathy 2024-07-01 criteria provided, single submitter clinical testing

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