ClinVar Miner

Submissions for variant nsv513783

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000011801 SCV000032034 pathogenic Non-syndromic X-linked intellectual disability 2008-05-01 no assertion criteria provided literature only
OMIM RCV000032597 SCV000056348 risk factor Autism, susceptibility to, X-linked 2 2008-05-01 no assertion criteria provided literature only

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