ClinVar Miner

Submissions for variant NM_173483.4(CYP4F22):c.939+15_939+40delinsTGGAGGGTGGAGCCCTGCCTGGGA

dbSNP: rs886054264
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000293637 SCV000411041 uncertain significance Congenital ichthyosiform erythroderma 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001723915 SCV001950520 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001723915 SCV004371469 likely benign not provided 2024-01-17 criteria provided, single submitter clinical testing

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