ClinVar Miner

Submissions for variant NM_004393.6(DAG1):c.255_258delinsCC (p.Leu86fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Wuerzburg RCV004698709 SCV005200273 likely pathogenic Autosomal recessive limb-girdle muscular dystrophy type 2P no assertion criteria provided clinical testing

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