Variants in gene NLRP3 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 8

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HGVS	dbSNP	gnomAD frequency
NM_001243133.2(NLRP3):c.2107C>A (p.Gln703Lys)	rs35829419	0.03262
NM_001243133.2(NLRP3):c.592G>A (p.Val198Met)	rs121908147	0.00835
NM_001243133.2(NLRP3):c.1463G>A (p.Arg488Lys)	rs145268073	0.00070
NM_001243133.2(NLRP3):c.1639A>T (p.Ser547Cys)	rs139833874	0.00061
NM_001243133.2(NLRP3):c.2855C>T (p.Thr952Met)	rs139814109	0.00051
NM_001243133.2(NLRP3):c.2176A>G (p.Ser726Gly)	rs147946775	0.00049
NM_001243133.2(NLRP3):c.1079T>A (p.Leu360Gln)	rs201593863	0.00012
NM_001243133.2(NLRP3):c.2419G>A (p.Ala807Thr)	rs201096167	0.00002

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