ClinVar Miner

Submissions for variant NM_080911.3(UNG):c.819A>G (p.Leu273=)

dbSNP: rs1593326380
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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 RCV001506327 SCV001711248 likely benign Hyper-IgM syndrome type 5 2018-11-24 criteria provided, single submitter clinical testing

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