{{Rsnum
|rsid=2670660
|Chromosome=17
|position=5615686
|Orientation=plus
|GMAF=0.337
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}linked to generalized [[vitiligo]]

{{PMID|17637824}} Individuals carrying high-risk alleles of both [[rs6502867]] and [[rs2670660]] had an odds ratio of 4.20 compared with individuals carrying a high-risk allele from only one signal.
{{PMID Auto
|PMID=21245836
|Title=The Missense Variation Q705K in CIAS1/NALP3/NLRP3 Gene and an NLRP1 Haplotype Are Associated With Celiac Disease
}}

{{PMID Auto
|PMID=22067658
|Title=Networks of intergenic long-range enhancers and snpRNAs drive castration-resistant phenotype of prostate cancer and contribute to pathogenesis of multiple common human disorders
|OA=1
}}

{{PMID Auto
|PMID=22235789
|Title=Polimorphisms in inflammasome genes are involved in the predisposition to systemic lupus erythematosus.
}}
{{PMID|19923886}} Identification of intergenic trans-regulatory RNAs containing a disease-linked SNP sequence and targeting cell cycle progression/differentiation pathways in multiple common human disorders.

{{PMID|20574744}} Genetic association of NALP1 with generalized vitiligo in Jordanian Arabs.

{{PMID|20697295}} Genetic predictors of glucocorticoid response in pediatric patients with inflammatory bowel diseases.

{{PMID|21149496}} NLRP1 influences the systemic sclerosis phenotype: a new clue for the contribution of innate immunity in systemic sclerosis-related fibrosing alveolitis pathogenesis.

{{PMID Auto
|PMID=23374100
|Title=Polymorphisms in NLRP1 gene and susceptibility to autoimmune thyroid disease.
}}

{{PMID Auto
|PMID=23773036
|Title=Association of NLRP1 genetic variants and mRNA overexpression with generalized vitiligo and disease activity in a Gujarat population.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}