ClinVar Miner

Submissions for variant GRCh37/hg19 9p13.3(chr9:36227245-36227455)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Medical Genetics, National & Kapodistrian University of Athens RCV003236714 SCV003935213 likely pathogenic GNE myopathy 2023-05-26 criteria provided, single submitter clinical testing

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