ClinVar Miner

Submissions for variant GRCh37/hg19 7q11.23(chr7:72744494-76038818)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV000767638 SCV000898260 pathogenic Williams syndrome 2018-11-01 criteria provided, single submitter clinical testing

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