ClinVar Miner

Submissions for variant PCDH15, 3-BP DEL, 5601AAC

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000005219 SCV000025397 pathogenic Usher syndrome type 1F 2005-03-01 no assertion criteria provided literature only
OMIM RCV000005220 SCV000025398 pathogenic USHER SYNDROME, TYPE ID/F, DIGENIC 2005-03-01 no assertion criteria provided literature only

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