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rs6502867

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0
Make rs6502867(C;C)
Make rs6502867(C;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position5517008
GeneNLRP1
is asnp
is mentioned by
dbSNPrs6502867
ebirs6502867
HLIrs6502867
Exacrs6502867
Varsomers6502867
Maprs6502867
PheGenIrs6502867
hapmaprs6502867
1000 genomesrs6502867
hgdprs6502867
ensemblrs6502867
gopubmedrs6502867
geneviewrs6502867
scholarrs6502867
googlers6502867
pharmgkbrs6502867
gwascentralrs6502867
openSNPrs6502867
23andMers6502867
23andMe allrs6502867
SNP Nexus

SNPshotrs6502867
SNPdbers6502867
MSV3drs6502867
GWAS Ctlgrs6502867
GMAF0.1483
Max Magnitude0
? (C;C) (C;T) (T;T) 28
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 19727120OA-icon.png] Fine-Mapping of Vitiligo Susceptibility Loci on Chromosomes 7 and 9 and Interactions with NLRP1 (NALP1)


[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 21331694] Evaluation of NLRP1 gene polymorphisms in Vogt-Koyanagi-Harada disease.


[PMID 21976003] NLRP1 gene polymorphism influences gene transcription and is a risk factor for rheumatoid arthritis in han chinese.


[PMID 23773036] Association of NLRP1 genetic variants and mRNA overexpression with generalized vitiligo and disease activity in a Gujarat population.