ClinVar Miner

Submissions for variant GRCh37/hg19 19p13.2(chr19:13363805-13363915)x1

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003223008 SCV003918191 likely pathogenic not provided 2023-03-01 criteria provided, single submitter clinical testing

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