ClinVar Miner

Submissions for variant NM_000246.4(CIITA):c.3318-8C>T

dbSNP: rs201115726
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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 RCV001474021 SCV001678185 likely benign MHC class II deficiency 2023-06-15 criteria provided, single submitter clinical testing

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