ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.1862del (p.Val621fs)

dbSNP: rs587776611
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000005032 SCV000025208 pathogenic Mowat-Wilson syndrome 2005-09-01 no assertion criteria provided literature only

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