ClinVar Miner

Submissions for variant CEP290, 4-BP DEL, 384TAGA

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000001405 SCV000021555 pathogenic Leber congenital amaurosis 10 2007-07-01 no assertion criteria provided literature only
OMIM RCV000033206 SCV000057052 pathogenic Meckel syndrome, type 4 2007-07-01 no assertion criteria provided literature only

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