ClinVar Miner

Submissions for variant NM_032578.4(MYPN):c.834A>G (p.Arg278=)

gnomAD frequency: 0.00001  dbSNP: rs2133996684
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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 RCV001437947 SCV001640813 likely benign Dilated cardiomyopathy 1KK 2022-08-16 criteria provided, single submitter clinical testing

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