Have questions? Visit https://www.reddit.com/r/SNPedia

rs2670660

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) normal
(A;G) 2.96x
(G;G) 2.74x
ReferenceGRCh38 38.1/141
Chromosome17
Position5615686
is asnp
is mentioned by
dbSNPrs2670660
ebirs2670660
HLIrs2670660
Exacrs2670660
Varsomers2670660
Maprs2670660
PheGenIrs2670660
hapmaprs2670660
1000 genomesrs2670660
hgdprs2670660
ensemblrs2670660
gopubmedrs2670660
geneviewrs2670660
scholarrs2670660
googlers2670660
pharmgkbrs2670660
gwascentralrs2670660
openSNPrs2670660
23andMers2670660
23andMe allrs2670660
SNP Nexus

SNPshotrs2670660
SNPdbers2670660
MSV3drs2670660
GWAS Ctlgrs2670660
GMAF0.337
Max Magnitude
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 22067658OA-icon.png] 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.