ClinVar Miner

Submissions for variant GRCh37/hg19 18p11.32(chr18:2682920-2803186)x3

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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 Goettingen RCV000787293 SCV000926229 uncertain significance Muscular Diseases 2019-04-04 no assertion criteria provided clinical testing

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