ClinVar Miner

Submissions for variant NM_032578.4(MYPN):c.3207C>T (p.Arg1069=)

gnomAD frequency: 0.00001  dbSNP: rs766738381
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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 RCV003086996 SCV003486118 likely benign Dilated cardiomyopathy 1KK 2024-02-16 criteria provided, single submitter clinical testing

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