ClinVar Miner

Submissions for variant GRCh37/hg19 4q31.3(chr4:151441408-151719830)

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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 RCV001195152 SCV001334112 pathogenic Combined immunodeficiency due to LRBA deficiency 2020-04-16 no assertion criteria provided clinical testing

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