ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.5923-12T>G

dbSNP: rs2148596650
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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 RCV002276220 SCV002564097 uncertain significance not provided 2021-06-01 criteria provided, single submitter clinical testing

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