ClinVar Miner

Submissions for variant NM_004070.4(CLCNKA):c.17G>A (p.Gly6Glu)

dbSNP: rs773206825
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Research Center, Shahid Beheshti University of Medical Sciences RCV000791098 SCV000930371 uncertain significance Bartter disease type 4B 2019-04-27 criteria provided, single submitter clinical testing

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