ClinVar Miner

Submissions for variant MECP2, 41-BP DEL, NT1157

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000012592 SCV000032827 pathogenic Rett syndrome, zappella variant 2003-03-01 no assertion criteria provided literature only
OMIM RCV000012593 SCV000032828 risk factor Autism, susceptibility to, X-linked 3 2003-03-01 no assertion criteria provided literature only

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