ClinVar Miner

Submissions for variant NM_000426.4(LAMA2):c.2834del (p.Gly945fs)

dbSNP: rs2114432671
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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 RCV001541905 SCV001760549 pathogenic Congenital muscular dystrophy no assertion criteria provided clinical testing

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