ClinVar Miner

Submissions for variant NM_139276.3(STAT3):c.1129G>A (p.Ala377Thr)

dbSNP: rs2081912356
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV001328610 SCV001519764 uncertain significance STAT3-related early-onset multisystem autoimmune disease 2020-05-06 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].

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