ClinVar Miner

Submissions for variant GRCh37/hg19 1q23.1(chr1:158655335-158667812)

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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 RCV001195114 SCV001334125 pathogenic Hereditary spherocytosis type 3 2020-04-16 no assertion criteria provided clinical testing

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