List of variants in gene NLRP3 reported as likely benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_001243133.2(NLRP3):c.1920C>T (p.Phe640=)	rs34698071	0.00230
NM_001243133.2(NLRP3):c.1119G>A (p.Glu373=)	rs138613962	0.00139
NM_001243133.2(NLRP3):c.930C>T (p.Asp310=)	rs143840033	0.00076
NM_001243133.2(NLRP3):c.2176A>G (p.Ser726Gly)	rs147946775	0.00049
NM_001243133.2(NLRP3):c.1245C>T (p.Ile415=)	rs139852370	0.00045
NM_001243133.2(NLRP3):c.1401C>T (p.Leu467=)	rs141637807	0.00029
NM_001243133.2(NLRP3):c.1665C>T (p.Asp555=)	rs151097783	0.00007
NM_001243133.2(NLRP3):c.111C>T (p.Ile37=)	rs145314485	0.00004
NM_001243133.2(NLRP3):c.2835-7T>G	rs747303698	0.00004
NM_001243133.2(NLRP3):c.2321+12T>A	rs747043119	0.00001
NM_001243133.2(NLRP3):c.2811C>T (p.Pro937=)	rs545121784	0.00001
NM_001243133.2(NLRP3):c.696C>A (p.Ile232=)	rs746712429	0.00001
NM_001243133.2(NLRP3):c.1011G>A (p.Lys337=)	rs766978634
NM_001243133.2(NLRP3):c.195G>A (p.Ala65=)	rs201205620
NM_001243133.2(NLRP3):c.2343G>T (p.Ser781=)	rs764753476
NM_001243133.2(NLRP3):c.51T>C (p.Asp17=)	rs1572151908

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