rs2670660
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | normal | |
| (A;G) | 2.96x | |
| (G;G) | 2.74x |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 5615686 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2670660 |
| dbSNP (classic) | rs2670660 |
| ClinGen | rs2670660 |
| ebi | rs2670660 |
| HLI | rs2670660 |
| Exac | rs2670660 |
| Gnomad | rs2670660 |
| Varsome | rs2670660 |
| LitVar | rs2670660 |
| Map | rs2670660 |
| PheGenI | rs2670660 |
| Biobank | rs2670660 |
| 1000 genomes | rs2670660 |
| hgdp | rs2670660 |
| ensembl | rs2670660 |
| geneview | rs2670660 |
| scholar | rs2670660 |
| rs2670660 | |
| pharmgkb | rs2670660 |
| gwascentral | rs2670660 |
| openSNP | rs2670660 |
| 23andMe | rs2670660 |
| SNPshot | rs2670660 |
| SNPdbe | rs2670660 |
| MSV3d | rs2670660 |
| GWAS Ctlg | rs2670660 |
| GMAF | 0.337 |
| Max Magnitude | 0 |
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 21245836] The Missense Variation Q705K in CIAS1/NALP3/NLRP3 Gene and an NLRP1 Haplotype Are Associated With Celiac Disease
[PMID 22067658
] Networks of intergenic long-range enhancers and snpRNAs drive castration-resistant phenotype of prostate cancer and contribute to pathogenesis of multiple common human disorders
[PMID 22235789] 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 23374100] Polymorphisms in NLRP1 gene and susceptibility to autoimmune thyroid disease.
[PMID 23773036] Association of NLRP1 genetic variants and mRNA overexpression with generalized vitiligo and disease activity in a Gujarat population.
[PMID 31448710] Frequency of Inflammasome Nlrp1/Nlrp3 Gene Receptor Polimorphisms And The Interleukins IL-1ß/IL-18 Gene Polymorphisms And Their Association With Severity Score In Sickle Cell Disease Patients.
