{{Rsnum
|rsid=4353135
|Gene=OR2B11
|Chromosome=1
|position=247453734
|Orientation=plus
|GMAF=0.3118
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=OR2B11
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 6.2 | 42.5 | 51.3
| HCB | 14.6 | 53.3 | 32.1
| JPT | 19.6 | 50.9 | 29.5
| YRI | 1.4 | 30.6 | 68.0
| ASW | 1.8 | 42.1 | 56.1
| CHB | 14.6 | 53.3 | 32.1
| CHD | 18.3 | 53.2 | 28.4
| GIH | 6.0 | 48.0 | 46.0
| LWK | 4.6 | 22.9 | 72.5
| MEX | 3.5 | 47.4 | 49.1
| MKK | 10.3 | 39.1 | 50.6
| TSI | 10.9 | 48.5 | 40.6
| HapMapRevision=28
}}{{omim
|desc=NLR FAMILY, PYRIN DOMAIN-CONTAINING 3; NLRP3
|id=606416
|rsnum=4353135
}}

{{omim
|id=266600
|rsnum=4353135
}}

{{PMID|19098911|OA=1
}} Common variants in the NLRP3 region contribute to Crohn's disease susceptibility.

{{PMID Auto
|PMID=23547871
|Title=Genetic variants in CARD8 but not in NLRP3 are associated with ankylosing spondylitis
}}

{{PMID Auto
|PMID=24295199
|Title=Association of NLRP3 and CARD8 genetic polymorphisms with juvenile idiopathic arthritis in a Taiwanese population
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}