ClinVar Miner

Submissions for variant NM_006736.6(DNAJB2):c.446-8G>A (rs3821039)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000545361 SCV000652825 benign Spinal muscular atrophy, distal, autosomal recessive, 5 2020-12-03 criteria provided, single submitter clinical testing
Molecular Genetics Laboratory,London Health Sciences Centre RCV001173853 SCV001336969 benign Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing
GeneDx RCV001653910 SCV001863236 benign not provided 2015-03-03 criteria provided, single submitter clinical testing

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