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rs3811021

From SNPedia

Orientationminus
Stabilizedminus
Make rs3811021(C;C)
Make rs3811021(C;T)
Make rs3811021(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position113814041
GeneAP4B1-AS1, PTPN22, RSBN1
is asnp
is mentioned by
dbSNPrs3811021
dbSNP (classic)rs3811021
ClinGenrs3811021
ebirs3811021
HLIrs3811021
Exacrs3811021
Gnomadrs3811021
Varsomers3811021
LitVarrs3811021
Maprs3811021
PheGenIrs3811021
Biobankrs3811021
1000 genomesrs3811021
hgdprs3811021
ensemblrs3811021
geneviewrs3811021
scholarrs3811021
googlers3811021
pharmgkbrs3811021
gwascentralrs3811021
openSNPrs3811021
23andMers3811021
SNPshotrs3811021
SNPdbers3811021
MSV3drs3811021
GWAS Ctlgrs3811021
GMAF0.1589
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 19503742OA-icon.png] Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients


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


[PMID 16478714OA-icon.png] Genotyping pooled DNA using 100K SNP microarrays: a step towards genomewide association scans.


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


[PMID 18075792OA-icon.png] PTPN22: its role in SLE and autoimmunity.


[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 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 19180477OA-icon.png] Genetic risk factors for rheumatoid arthritis differ in Caucasian and Korean populations.


[PMID 24386393OA-icon.png] Genetic Heterogeneity of Susceptibility Gene in Different Ethnic Populations: Refining Association Study of PTPN22 for Graves' Disease in a Chinese Han Population