ClinVar Miner

Submissions for variant GRCh37/hg19 4q25(chr4:111528916-111888401)x1

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetics and Molecular Pathology, SA Pathology RCV000416499 SCV000494276 pathogenic Axenfeld-Rieger syndrome type 1 2013-07-12 no assertion criteria provided clinical testing

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