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rs1310182

From SNPedia

Orientationminus
Stabilizedminus
Make rs1310182(C;C)
Make rs1310182(C;T)
Make rs1310182(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position113830881
GenePTPN22, RP5-1073O3.2
is asnp
is mentioned by
dbSNPrs1310182
ebirs1310182
HLIrs1310182
Exacrs1310182
Varsomers1310182
Maprs1310182
PheGenIrs1310182
hapmaprs1310182
1000 genomesrs1310182
hgdprs1310182
ensemblrs1310182
gopubmedrs1310182
geneviewrs1310182
scholarrs1310182
googlers1310182
pharmgkbrs1310182
gwascentralrs1310182
openSNPrs1310182
23andMers1310182
23andMe allrs1310182
SNP Nexus

SNPshotrs1310182
SNPdbers1310182
MSV3drs1310182
GWAS Ctlgrs1310182
GMAF0.4614
Max Magnitude

[PMID 20510318] Association of PTPN22 Haplotypes with Type 1 Diabetes in the Japanese Population


[PMID 20615141] Association of the Protein Tyrosine Phosphatase Nonreceptor 22 Haplotypes with Autoimmune Thyroid Disease in the Japanese Population

[PMID 16175503OA-icon.png] PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis.

[PMID 17934143] Further evidence of a primary, causal association of the PTPN22 620W variant with type 1 diabetes.

[PMID 18341666OA-icon.png] Polymorphisms in the PTPN22 region are associated with psoriasis of early onset.

[PMID 18466461OA-icon.png] Meta-genetic association of rheumatoid arthritis and PTPN22 using PedGenie 2.1.

[PMID 18466529OA-icon.png] Comparing strategies for evaluation of candidate genes in case-control studies using family data.

[PMID 18466531OA-icon.png] Case-control association analysis of rheumatoid arthritis with candidate genes using related cases.

[PMID 18466575OA-icon.png] Comparison of the power of haplotype-based versus single- and multilocus association methods for gene x environment (gene x sex) interactions and application to gene x smoking and gene x sex interactions in rheumatoid arthritis.

[PMID 21193990] A PTPN22 promoter polymorphism -1123G>C is associated with RA pathogenesis in Chinese.

[PMID 22396730OA-icon.png] No association of PTPN22 polymorphisms with susceptibility to ocular Behcet's disease in two Chinese Han populations.


[PMID 25073032] Association Between a Gain-of-Function Variant of PTPN22 and Rejection in Liver Transplantation


[PMID 27888068] Associations of single nucleotide polymorphisms of PTPN22 and Ctla4 genes with the risk of allergic rhinitis in a Chinese Han population.