ClinVar Miner

Submissions for variant NM_020433.5(JPH2):c.534C>T (p.Asp178=)

dbSNP: rs2515745163
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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 RCV002583098 SCV002939131 likely benign Hypertrophic cardiomyopathy 2022-03-06 criteria provided, single submitter clinical testing

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