ClinVar Miner

Submissions for variant NM_000085.5(CLCNKB):c.968+47T>C

dbSNP: rs7368166
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001579036 SCV001806427 benign Bartter disease type 4B 2021-07-22 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001579037 SCV001806428 benign Bartter disease type 3 2021-07-22 criteria provided, single submitter clinical testing
GeneDx RCV001615340 SCV001834731 benign not provided 2018-11-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001615340 SCV005283176 benign not provided criteria provided, single submitter not provided

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