List of variants in gene NLRP3 reported as benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001243133.2(NLRP3):c.657C>T (p.Thr219=)	rs7525979	0.10943
NM_001243133.2(NLRP3):c.1302C>T (p.Ser434=)	rs34298354	0.08679
NM_001243133.2(NLRP3):c.2107C>A (p.Gln703Lys)	rs35829419	0.03262
NM_001243133.2(NLRP3):c.423C>T (p.Tyr141=)	rs56710146	0.00680
NM_001243133.2(NLRP3):c.1231C>T (p.Leu411=)	rs148478875	0.00638
NM_001243133.2(NLRP3):c.1600C>T (p.Leu534=)	rs116054301	0.00596
NM_001243133.2(NLRP3):c.1020C>T (p.Pro340=)	rs41311573	0.00548
NM_001243133.2(NLRP3):c.1389C>T (p.His463=)	rs111400208	0.00354
NM_001243133.2(NLRP3):c.1920C>T (p.Phe640=)	rs34698071	0.00230
NM_001243133.2(NLRP3):c.207C>T (p.Ala69=)	rs200082602	0.00005
NM_001243133.2(NLRP3):c.726G>A (p.Ala242=)	rs3806268

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