ClinVar Miner

Submissions for variant NM_152336.4(AGBL1):c.3323+1G>A

dbSNP: rs79072327
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV002249234 SCV002517531 uncertain significance Corneal dystrophy, Fuchs endothelial, 8 2023-12-12 criteria provided, single submitter clinical testing

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