ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.1790+8_1790+9del

dbSNP: rs2142860055
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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 RCV001430175 SCV001632905 likely benign Hypertrophic cardiomyopathy 2019-01-31 criteria provided, single submitter clinical testing

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