ClinVar Miner

Submissions for variant NM_000495.5(COL4A5):c.609+21T>C (rs6622333)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000507882 SCV000603153 benign not specified 2016-08-15 criteria provided, single submitter clinical testing
Research and Development, ARUP Laboratories RCV000021174 SCV000041840 benign Alport syndrome 1, X-linked recessive 2012-12-04 no assertion criteria provided clinical testing Converted during submission to Benign.

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