ClinVar Miner

Submissions for variant NM_032578.4(MYPN):c.3493+6G>A

dbSNP: rs750903219
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000439887 SCV000519027 likely benign not specified 2015-10-01 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Labcorp Genetics (formerly Invitae), Labcorp RCV000462682 SCV000553458 uncertain significance Dilated cardiomyopathy 1KK 2021-08-27 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV000439887 SCV001918052 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001727720 SCV001969619 likely benign not provided no assertion criteria provided clinical testing

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