ClinVar Miner

Submissions for variant NM_000246.4(CIITA):c.2657+4G>A

dbSNP: rs1596557195
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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 RCV000814049 SCV000954441 uncertain significance MHC class II deficiency 2021-09-01 criteria provided, single submitter clinical testing

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