ClinVar Miner

Submissions for variant GRCh37/hg19 17p13.3(chr17:468095-661692)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. RCV002281679 SCV002568444 uncertain significance Congenital omphalocele no assertion criteria provided clinical testing

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