ClinVar Miner

Submissions for variant NM_000231.3(SGCG):c.95G>A (p.Arg32Lys)

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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 RCV003326231 SCV004032331 uncertain significance Autosomal recessive limb-girdle muscular dystrophy type 2C no assertion criteria provided clinical testing

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