ClinVar Miner

Submissions for variant NM_020971.3(SPTBN4):c.2903+2T>C

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre RCV003990429 SCV004807057 likely pathogenic Neurodevelopmental disorder with hypotonia, neuropathy, and deafness 2024-03-26 criteria provided, single submitter clinical testing

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