ClinVar Miner

Submissions for variant NM_138636.5(TLR8):c.2498T>C (p.Phe833Ser)

dbSNP: rs997809680
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomics Facility, Ludwig-Maximilians-Universität München RCV001824552 SCV002074124 uncertain significance Autoimmune hemolytic anemia; Systemic autoinflammation 2022-02-08 criteria provided, single submitter clinical testing

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