ClinVar Miner

Submissions for variant NM_001243133.2(NLRP3):c.29G>T (p.Arg10Met)

dbSNP: rs2103083622
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Seattle Children's Hospital Molecular Genetics Laboratory, Seattle Children's Hospital RCV003486475 SCV004240773 pathogenic Cerebral arteriovenous malformation no assertion criteria provided clinical testing

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