ClinVar Miner

Submissions for variant NM_000152.5(GAA):c.1755-4C>T

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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 RCV002281213 SCV002569370 uncertain significance Muscular dystrophy no assertion criteria provided clinical testing

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