ClinVar Miner

Submissions for variant NM_001830.4(CLCN4):c.1709G>A (p.Gly570Asp)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center RCV003233395 SCV003932224 uncertain significance not provided 2023-03-28 criteria provided, single submitter clinical testing PM2, PP2, PP3

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