ClinVar Miner

Submissions for variant NM_001330311.2(DVL1):c.363-1G>C

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
MGZ Medical Genetics Center RCV002289257 SCV002579215 likely pathogenic Autosomal dominant Robinow syndrome 2 2022-05-20 criteria provided, single submitter clinical testing

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