ClinVar Miner

Submissions for variant NM_020433.5(JPH2):c.1437G>T (p.Arg479=)

dbSNP: rs2145838750
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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 RCV001433977 SCV001636775 likely benign Hypertrophic cardiomyopathy 2023-05-15 criteria provided, single submitter clinical testing

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