List of variants in gene NLRP3 reported as likely pathogenic for Chronic infantile neurological, cutaneous and articular syndrome

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001243133.2(NLRP3):c.1054G>A (p.Ala352Thr)	rs180177503
NM_001243133.2(NLRP3):c.2263G>C (p.Gly755Arg)	rs180177469
NM_001243133.2(NLRP3):c.779G>C (p.Arg260Pro)	rs180177442

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