ClinVar Miner

Submissions for variant NM_001025603.2(RFX5):c.33C>T (p.Pro11=)

dbSNP: rs2102071618
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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 RCV002182253 SCV002338005 likely benign MHC class II deficiency 2021-07-15 criteria provided, single submitter clinical testing

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