ClinVar Miner

Submissions for variant NM_001377458.1(CLCC1):c.231+14T>A

gnomAD frequency: 0.00001  dbSNP: rs748602461
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002090357 SCV002330781 likely benign not provided 2024-04-09 criteria provided, single submitter clinical testing

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