ClinVar Miner

Submissions for variant NM_004070.4(CLCNKA):c.1929+30C>A

dbSNP: rs10927892
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001579088 SCV001806491 benign Bartter disease type 4B 2021-07-22 criteria provided, single submitter clinical testing
GeneDx RCV001658300 SCV001873382 benign not provided 2018-11-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001658300 SCV005282684 benign not provided criteria provided, single submitter not provided

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