List of variants in gene NLRP3 reported as likely 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: 23

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HGVS	dbSNP	gnomAD frequency
NM_001243133.2(NLRP3):c.592G>A (p.Val198Met)	rs121908147	0.00835
NM_001243133.2(NLRP3):c.2151-7T>C	rs116546330	0.00084
NM_001243133.2(NLRP3):c.2488C>A (p.Leu830Ile)	rs114158404	0.00083
NM_001243133.2(NLRP3):c.930C>T (p.Asp310=)	rs143840033	0.00076
NM_001243133.2(NLRP3):c.3048A>C (p.Leu1016Phe)	rs143548979	0.00068
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.203T>C (p.Met68Thr)	rs147559626	0.00048
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.674C>T (p.Ala225Val)	rs180177493	0.00019
NM_001243133.2(NLRP3):c.2364C>A (p.Ile788=)	rs766840708	0.00013
NM_001243133.2(NLRP3):c.906C>T (p.Phe302=)	rs756989752	0.00011
NM_001243133.2(NLRP3):c.225G>A (p.Ala75=)	rs140219362	0.00007
NM_001243133.2(NLRP3):c.2424C>T (p.Leu808=)	rs147154764	0.00005
NM_001243133.2(NLRP3):c.1269G>A (p.Gln423=)	rs201035625	0.00002
NM_001243133.2(NLRP3):c.1629C>T (p.Asn543=)
NM_001243133.2(NLRP3):c.1698C>T (p.Phe566=)
NM_001243133.2(NLRP3):c.1899C>T (p.Tyr633=)	rs200089426
NM_001243133.2(NLRP3):c.2185C>A (p.Arg729=)	rs148590318
NM_001243133.2(NLRP3):c.2322-5T>C
NM_001243133.2(NLRP3):c.2337C>G (p.Gly779=)

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