ClinVar Miner

Submissions for variant NM_032578.4(MYPN):c.3543C>T (p.Cys1181=)

gnomAD frequency: 0.00001  dbSNP: rs756337136
Minimum review status: Collection method:
Minimum conflict level:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001393916 SCV001595593 likely benign Dilated cardiomyopathy 1KK 2025-07-20 criteria provided, single submitter clinical testing

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