ClinVar Miner

Submissions for variant GRCh37/hg19 12p12.2-12.1(chr12:21017576-21404166)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Molecular and Human Genetics, Baylor College of Medicine RCV001195113 SCV001334124 pathogenic Rotor syndrome 2020-04-16 no assertion criteria provided clinical testing

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