ClinVar Miner

Submissions for variant NM_000246.4(CIITA):c.1044G>T (p.Thr348=)

dbSNP: rs140683241
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001280289 SCV001699986 likely benign MHC class II deficiency 2023-12-19 criteria provided, single submitter clinical testing
Natera, Inc. RCV001280289 SCV001467455 uncertain significance MHC class II deficiency 2020-04-24 no assertion criteria provided clinical testing

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