ClinVar Miner

Submissions for variant NM_013447.4(ADGRE2):c.1276C>T (p.Gln426Ter)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetics and Genomic Medicine Centre, NeuroGen Healthcare, NeuroGen Healthcare RCV005232608 SCV005873799 likely pathogenic Vibratory urticaria 2021-11-17 criteria provided, single submitter clinical testing

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