ClinVar Miner

Submissions for variant NM_000246.4(CIITA):c.1857G>A (p.Gln619=)

dbSNP: rs2144722976
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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 RCV002198148 SCV002360507 likely benign MHC class II deficiency 2021-05-21 criteria provided, single submitter clinical testing

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