ClinVar Miner

Submissions for variant NM_020433.5(JPH2):c.255G>A (p.Glu85=)

dbSNP: rs2515764205
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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 RCV003587253 SCV004285098 likely benign Hypertrophic cardiomyopathy 2023-10-13 criteria provided, single submitter clinical testing

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