ClinVar Miner

Submissions for variant GRCh37/hg19 Xp21.1(chrX:31881035-31993637)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Cytogenetics and Genomic Microarray, ARUP Laboratories RCV002052803 SCV002319912 likely pathogenic not specified 2022-03-01 criteria provided, single submitter clinical testing

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