ClinVar Miner

Submissions for variant NM_024782.3(NHEJ1):c.837C>A (p.Gly279=)

gnomAD frequency: 0.00010  dbSNP: rs145592698
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000978645 SCV001126577 likely benign Cernunnos-XLF deficiency 2023-12-06 criteria provided, single submitter clinical testing

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