ClinVar Miner

Submissions for variant NM_198576.4(AGRN):c.2536+45C>T

gnomAD frequency: 0.00658  dbSNP: rs183108359
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000252843 SCV000317024 likely benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001552513 SCV001773214 likely benign not provided 2019-02-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001552513 SCV005263944 likely benign not provided criteria provided, single submitter not provided

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