ClinVar Miner

Submissions for variant NM_000091.4(COL4A3):c.1909G>A (p.Gly637Arg) (rs761686437)

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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 RCV000256394 SCV000323166 uncertain significance Alport syndrome, autosomal recessive no assertion criteria provided clinical testing

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