ClinVar Miner

Submissions for variant NM_004070.4(CLCNKA):c.867-8C>T

gnomAD frequency: 0.00011  dbSNP: rs200325856
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000893349 SCV001037276 benign not provided 2018-03-29 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002501481 SCV002798136 benign Bartter disease type 4B 2022-03-09 criteria provided, single submitter clinical testing

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