ClinVar Miner

Submissions for variant NC_000023.10:g.31973924_32017000dup

Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Rare Disease Group, Clinical Genetics,Karolinska Institutet RCV000787470 SCV000926432 likely pathogenic Muscle dystrophy 2019-04-09 no assertion criteria provided clinical testing

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