ClinVar Miner

Submissions for variant NC_000023.10:g.153296106_153296275delins[NC_000008.10:g.50305003_50392184inv;TTACACAG]

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Research Centre for Medical Genetics,Federal State Budgetary Scientific Institution RCV001171507 SCV001334294 pathogenic Rett syndrome 2018-01-01 criteria provided, single submitter case-control

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