ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.7009T>G (p.Leu2337Val)

dbSNP: rs1603513931
Minimum review status: Collection method:
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV000999371 SCV001155956 uncertain significance not provided 2016-06-01 criteria provided, single submitter clinical testing

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