ClinVar Miner

Submissions for variant NM_003588.3(CUL4B):c.1906+1G>T (rs797044862)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000190824 SCV000245694 pathogenic Syndromic X-linked mental retardation, Cabezas type 2015-01-01 no assertion criteria provided literature only

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