ClinVar Miner

Submissions for variant NM_198576.4(AGRN):c.4879+32G>A

gnomAD frequency: 0.55443  dbSNP: rs2799067
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000242423 SCV000317062 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001711755 SCV001946079 benign not provided 2019-08-28 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001711755 SCV005286020 benign not provided criteria provided, single submitter not provided

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