ClinVar Miner

Submissions for variant NM_000246.4(CIITA):c.2400A>T (p.Thr800=)

dbSNP: rs750834114
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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 RCV002172112 SCV002334327 likely benign MHC class II deficiency 2021-03-13 criteria provided, single submitter clinical testing

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