ClinVar Miner

Submissions for variant NM_001498.4(GCLC):c.264-11C>A

gnomAD frequency: 0.00018  dbSNP: rs199775302
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001810583 SCV001474291 uncertain significance not provided 2020-06-26 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001810583 SCV002444230 likely benign not provided 2024-05-17 criteria provided, single submitter clinical testing

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