ClinVar Miner

Submissions for variant NM_001098629.3(IRF5):c.-12+198=

gnomAD frequency: 0.47453  dbSNP: rs1432329681
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000003564 SCV000023722 risk factor Systemic lupus erythematosus, susceptibility to, 10 2008-03-15 no assertion criteria provided literature only
OMIM RCV000003565 SCV000023723 pathogenic Rheumatoid arthritis 2008-03-15 no assertion criteria provided literature only

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