ClinVar Miner

Submissions for variant NM_000448.2(RAG1):c.2880A>G (p.Ala960=) (rs1980131)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000250266 SCV000304367 benign not specified criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000297247 SCV000371696 likely benign Severe Combined Immune Deficiency 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000370544 SCV000371697 likely benign Histiocytic medullary reticulosis 2016-06-14 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000755380 SCV000604999 benign not provided 2017-05-09 criteria provided, single submitter clinical testing

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