ClinVar Miner

Submissions for variant GRCh37/hg19 2q13(chr2:110504318-111365996)x1

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Cytogenetics and Genomic Microarray, ARUP Laboratories RCV003986326 SCV004802455 uncertain significance not specified criteria provided, single submitter clinical testing
Cytogenetics, Genetics Associates, Inc. RCV002285057 SCV002571734 uncertain significance Tetralogy of Fallot no assertion criteria provided clinical testing
Cytogenetics, Genetics Associates, Inc. RCV002305676 SCV002574758 pathogenic See cases no assertion criteria provided clinical testing

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