ClinVar Miner

Submissions for variant NM_024782.3(NHEJ1):c.707-8G>A

dbSNP: rs1574697770
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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 RCV001488441 SCV001692958 likely benign Cernunnos-XLF deficiency 2021-04-09 criteria provided, single submitter clinical testing

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