ClinVar Miner

Submissions for variant NM_000246.4(CIITA):c.174A>T (p.Gly58=)

dbSNP: rs759412177
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV002504404 SCV002816375 uncertain significance MHC class II deficiency; Rheumatoid arthritis 2021-09-28 criteria provided, single submitter clinical testing
Natera, Inc. RCV001279100 SCV001466164 uncertain significance MHC class II deficiency 2020-10-05 no assertion criteria provided clinical testing

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