ClinVar Miner

Submissions for variant GRCh37/hg19 16p11.2(chr16:29567296-30177807)x1

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ISCA site 1 RCV000511641 SCV000585742 pathogenic See cases 2015-04-19 no assertion criteria provided clinical testing
Cytogenetics, Genetics Associates, Inc. RCV002282737 SCV002568439 uncertain significance Dysmorphic features no assertion criteria provided clinical testing

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