ClinVar Miner

Submissions for variant NM_032578.4(MYPN):c.3936G>A (p.Arg1312=)

gnomAD frequency: 0.00001  dbSNP: rs1199855737
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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 RCV003842910 SCV004642447 likely benign Dilated cardiomyopathy 1KK 2022-11-13 criteria provided, single submitter clinical testing

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