ClinVar Miner

Submissions for variant NM_000246.4(CIITA):c.2406G>T (p.Arg802=)

dbSNP: rs948508818
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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 RCV002157718 SCV002413183 likely benign MHC class II deficiency 2021-09-15 criteria provided, single submitter clinical testing

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