ClinVar Miner

Submissions for variant NM_001110792.2(MECP2):c.*9G>T

dbSNP: rs144008995
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Children's Hospital of Philadelphia RCV000678232 SCV000804252 uncertain significance not provided 2015-04-03 no assertion criteria provided clinical testing

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