ClinVar Miner

Submissions for variant NM_000246.4(CIITA):c.358+19G>A

dbSNP: rs2038398049
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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 RCV003636328 SCV004392128 likely benign MHC class II deficiency 2023-01-11 criteria provided, single submitter clinical testing

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