ClinVar Miner

Submissions for variant NM_001142784.3(IL11RA):c.72C>T (p.Ser24=)

gnomAD frequency: 0.00670  dbSNP: rs34893971
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000501926 SCV000595225 likely benign not specified 2016-07-22 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000895876 SCV001039942 benign not provided 2023-12-17 criteria provided, single submitter clinical testing
GeneDx RCV000895876 SCV001947425 benign not provided 2020-09-01 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000895876 SCV005226348 likely benign not provided criteria provided, single submitter not provided

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