ClinVar Miner

Submissions for variant NG_011787.1:g.(205313_260238)_(334455_354191)del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000477967 SCV000564400 pathogenic Chromosome 1p32-p31 deletion syndrome 2014-02-01 no assertion criteria provided literature only

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