ClinVar Miner

Submissions for variant NM_003745.2(SOCS1):c.64C>T (p.Arg22Trp)

dbSNP: rs2069586831
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Immunogenetics of Pediatric Autoimmune Diseases, Institut Imagine RCV001254900 SCV001430916 likely pathogenic Systemic lupus erythematosus 2020-01-01 no assertion criteria provided research
OMIM RCV001526872 SCV001737562 pathogenic AUTOINFLAMMATORY SYNDROME, FAMILIAL, WITHOUT IMMUNODEFICIENCY 2021-06-17 no assertion criteria provided literature only

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