ClinVar Miner

Submissions for variant GRCh37/hg19 10q25.3-26.12(chr10:118891670-122349064)x1

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Leipzig Medical Center RCV001801230 SCV002047442 uncertain significance Astigmatism; Congenital ocular coloboma; Patent foramen ovale; Premature birth; Abnormality of the face 2020-11-27 criteria provided, single submitter clinical testing

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