ClinVar Miner

Submissions for variant NM_001211.5(BUB1B):c.2386-11A>G

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000023213 SCV000044504 pathogenic Mosaic variegated aneuploidy syndrome 1 2010-12-30 no assertion criteria provided literature only
OMIM RCV000023214 SCV000044505 affects Premature chromatid separation trait 2010-12-30 no assertion criteria provided literature only

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