ClinVar Miner

Submissions for variant NM_001830.4(CLCN4):c.1577-6T>C

gnomAD frequency: 0.00004  dbSNP: rs770995887
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 RCV000864192 SCV001004962 benign not provided 2024-10-09 criteria provided, single submitter clinical testing
GeneDx RCV000864192 SCV001842743 benign not provided 2020-04-02 criteria provided, single submitter clinical testing

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