ClinVar Miner

Submissions for variant NM_139284.3(LGI4):c.*11G>A

gnomAD frequency: 0.34468  dbSNP: rs11084800
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001597824 SCV001831345 benign not provided 2021-05-12 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001730860 SCV001981347 benign Arthrogryposis multiplex congenita 1, neurogenic, with myelin defect 2021-08-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001597824 SCV005314880 benign not provided criteria provided, single submitter not provided

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