ClinVar Miner

Submissions for variant NM_001389.5(DSCAM):c.651A>G (p.Val217=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003431508 SCV004153675 benign not provided 2022-06-01 criteria provided, single submitter clinical testing DSCAM: BS1, BS2
PreventionGenetics, part of Exact Sciences RCV003954172 SCV004766569 benign DSCAM-related disorder 2022-01-31 no assertion criteria provided clinical testing This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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