ClinVar Miner

Submissions for variant GRCh37/hg19 12q21.31(chr12:83765377-84013252)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics, Erasmus University Medical Center RCV000416684 SCV000266694 likely benign Abnormality of esophagus morphology 2015-12-15 criteria provided, single submitter research

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