{{Rsnum
|rsid=6672995
|Chromosome=1
|position=247457731
|Orientation=plus
|GMAF=0.1322
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 5.4 | 24.1 | 70.5
| HCB | 0.0 | 8.0 | 92.0
| JPT | 0.9 | 21.4 | 77.7
| YRI | 0.0 | 8.8 | 91.2
| ASW | 5.3 | 22.8 | 71.9
| CHB | 0.0 | 8.0 | 92.0
| CHD | 0.9 | 9.2 | 89.9
| GIH | 2.0 | 10.9 | 87.1
| LWK | 0.0 | 10.0 | 90.0
| MEX | 5.2 | 36.2 | 58.6
| MKK | 1.3 | 23.7 | 75.0
| TSI | 4.9 | 29.4 | 65.7
| HapMapRevision=28
}}{{omim
|desc=NLR FAMILY, PYRIN DOMAIN-CONTAINING 3; NLRP3
|id=606416
|rsnum=6672995
}}

{{omim
|id=266600
|rsnum=6672995
}}

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

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}