ClinVar Miner

Submissions for variant NM_212482.4(FN1):c.7144+1G>A

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Goettingen RCV002281673 SCV002570097 likely pathogenic Glomerulopathy with fibronectin deposits 2 2022-09-09 no assertion criteria provided clinical testing

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