ClinVar Miner

Submissions for variant NM_001127898.4(CLCN5):c.*3652T>C

gnomAD frequency: 0.12053  dbSNP: rs56657044
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000368809 SCV000482578 benign Dent disease 2016-06-14 criteria provided, single submitter clinical testing

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