ClinVar Miner

Submissions for variant GRCh37/hg19 Yp11.31-11.2(chrY:2650140-9651417)x1

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Cytogenetics, Genetics Associates, Inc. RCV002287643 SCV002577650 pathogenic Klinefelter syndrome no assertion criteria provided clinical testing

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