ClinVar Miner

Submissions for variant NM_033380.3(COL4A5):c.4706+4A>C (rs1569508999)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Bioscientia Institut fuer Medizinische Diagnostik GmbH,Sonic Healthcare RCV000735675 SCV000863818 uncertain significance Alport syndrome 1, X-linked recessive 2018-02-19 no assertion criteria provided clinical testing

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