ClinVar Miner

Submissions for variant NM_000246.4(CIITA):c.199+89C>T

dbSNP: rs11074937
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
Genome-Nilou Lab RCV001543003 SCV001761449 benign MHC class II deficiency 2021-07-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004715484 SCV005289569 benign not provided criteria provided, single submitter not provided

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